FDA 510(k)
FDA class 1
Substantially Equivalent
🇺🇸 United States
SCANMATE III
K Number: K921878
·
Decision Sep 11, 1992
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
2
Applicant Total
13
Review Days
144
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Basic Information
- Device Name
- SCANMATE III
- K Number
- K921878
- Device Class
- FDA class 1
- Clearance Type
- Traditional
- Regulation Number
- 892.1370
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Statement or Summary
- Summary
- Applicant
- Circadian, Inc.
- Date Received
- April 20, 1992
- Decision Date
- September 11, 1992
- Product Code
- IYP
- 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 |
|---|---|---|---|
| IYP | Phantom, Anthropomorphic, Nuclear | FDA class 1 | Radiology |
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Other Clearances by Circadian, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K894956 | CIRCAMED HOLTER VERSION 4 | Feb 5, 1990 | Substantially Equivalent |
| K874641 | CIRCADIAN STRESS TEST II | Apr 1, 1988 | Substantially Equivalent |
| K874155 | CIRCAMED MONITOR REMOTE START CONDUCTANCE METER | Nov 23, 1987 | Substantially Equivalent |
| K871251 | CIRCAMED FULL DISCLOSURE SYSTEM | May 22, 1987 | Substantially Equivalent |
| K860973 | CIRCADIAN STRESS TEST SYSTEM | Aug 25, 1986 | Substantially Equivalent |
| K851517 | CIRCA MED SINGLE-CHANNEL-AMBULATORY CARDIAC MONITO | Oct 2, 1985 | Substantially Equivalent |
| K851643 | REMOTE CONTROL MODULE | Sep 9, 1985 | Substantially Equivalent |
| K840741 | PULMONARY FUNCTION TESTING STS | Mar 5, 1984 | Substantially Equivalent |
| K833619 | CONDUCTANCE METER | Jan 27, 1984 | Substantially Equivalent |
| K830830 | CIRCA MED TWO-CHANNEL | Jun 18, 1983 | Substantially Equivalent |