FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
ULTRASONIC STETHOSCOPE
K Number: K803246
·
Decision Jan 28, 1981
Classifications
1
FEI Numbers
220
Registration Numbers
220
Same Product Code
1171
Applicant Total
18
Review Days
36
Research this 510(k) in seconds
The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.
Free to try · every answer cites its records
Basic Information
- Device Name
- ULTRASONIC STETHOSCOPE
- K Number
- K803246
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1550
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Applicant
- Sonicaid, Inc.
- Date Received
- December 23, 1980
- Decision Date
- January 28, 1981
- Product Code
- IYN
- Advisory Committee
- Radiology
- Review Advisory Committee
- RA
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| IYN | System, Imaging, Pulsed Doppler, Ultrasonic | FDA class 2 | Radiology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (IYN), ordered by most recent decision date.
ACUSON Sequoia Diagnostic Ultrasound System;ACUSON Sequoia Select Diagnostic Ultrasound System;ACUSON Origin Diagnostic Ultrasound System;ACUSON Origin ICE Diagnostic Ultrasound System
FDA 510(k)
FDA Class 2
·Radiology
ES-Series
FDA 510(k)
FDA Class 2
·Radiology
EPIQ Series Diagnostic Ultrasound System
FDA 510(k)
FDA Class 2
·Radiology
EPIQ Series Diagnostic Ultrasound Systems; Affiniti Series Diagnostic Ultrasound Systems
FDA 510(k)
FDA Class 2
·Radiology
LOGIQ e
FDA 510(k)
FDA Class 2
·Radiology
SonoPort Series Digital Color Doppler Ultrasound System (SonoPort 1, SonoPort 1 Exp, SonoPort 1 Pro, SonoPort 1 Elite, SonoPort 1 Plus, SonoPort 2, SonoPort 2 Exp, SonoPort 2 Pro, SonoPort 2 Elite, SonoPort 2 Plus, SonoPort 3, SonoPort 3 Exp, SonoPort 3 Pro, SonoPort 3 Elite, SonoPort 3 Plus, SonoPort 4, SonoPort 4 Exp, SonoPort 4 Pro, SonoPort 4 Elite, SonoPort 4 Plus, SonoPort 5, SonoPort 5 Exp, SonoPort 5 Pro, SonoPort 5 Elite, SonoPort 5 Plus, SonoPort 6, SonoPort 6 Exp, SonoPort 6
FDA 510(k)
FDA Class 2
·Radiology
Other Clearances by Sonicaid, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K873673 | BV105 (&BV105R) VASCULAR FLOW DETECTOR W/OPTIONAL | Feb 26, 1988 | Substantially Equivalent |
| K872074 | 5 MHZ TRANSDUCER | Aug 25, 1987 | Substantially Equivalent |
| K863803 | VASOPULSE(TM)/MODEL 5000 | May 6, 1987 | Substantially Equivalent |
| K862720 | VASOFLO-3 & EXTRAVASCULAR BLOOD FLOW PROBES | Nov 17, 1986 | Substantially Equivalent |
| K861237 | VASOVIEW DUPLEX IMAGING SYSTEM | Jul 14, 1986 | Substantially Equivalent for Some Indications |
| K851102 | VASOSCREEN IMPEDANCE PLETHYSMOGRAPH | May 16, 1985 | Substantially Equivalent |
| K833902 | VASOSCAN | Jan 27, 1984 | Substantially Equivalent |
| K832374 | PHOTOFLO DUAL-MODE PHOTOPLETHYSMOGRAPH | Dec 1, 1983 | Substantially Equivalent |
| K833488 | SONICOMP | Nov 28, 1983 | Substantially Equivalent |
| K833227 | SONICAID MODEL D206E AIR EMBOLI-DETECT | Oct 27, 1983 | Substantially Equivalent |