FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
XENON DELIVERY SYSTEM
K Number: K820143
·
Decision Mar 2, 1982
Classifications
1
FEI Numbers
12
Registration Numbers
12
Same Product Code
47
Applicant Total
75
Review Days
42
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Basic Information
- Device Name
- XENON DELIVERY SYSTEM
- K Number
- K820143
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 892.1390
- Medical Specialty
- Radiology
- Decision
- Substantially Equivalent
- Applicant
- Vital Signs, Inc.
- Date Received
- January 19, 1982
- Decision Date
- March 2, 1982
- Product Code
- IYT
- 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 |
|---|---|---|---|
| IYT | System, Rebreathing, Radionuclide | FDA class 2 | Radiology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (IYT), ordered by most recent decision date.
Patient Administration Set
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XENON CIRCUIT
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XENON CIRCUIT
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TETLEY PATIENT ADMINISTRATION SET
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BOLUS XENON CIRCUIT
FDA 510(k)
FDA Class 2
·Radiology
Other Clearances by Vital Signs, Inc.
| K Number | Device Name | ||
|---|---|---|---|
| K112902 | ENFLOW IV FLUID WARMER | Mar 14, 2012 | Substantially Equivalent |
| K041309 | IMASK TM | Jun 30, 2004 | Substantially Equivalent |
| K030985 | BREAS PV 10I CPAP SYSTEM, MODEL PV 10I | Oct 15, 2003 | Substantially Equivalent |
| K022402 | DISPOSABLE PRESSURE MANOMETER | Aug 22, 2002 | Substantially Equivalent |
| K021315 | SURE-LOK | Aug 21, 2002 | Substantially Equivalent |
| K002454 | BREAS HA50 HUMIDIFIER, MODEL HA50 | Mar 7, 2001 | Substantially Equivalent |
| K001553 | BREAS PV 100 CPAP SYSTEM | Aug 3, 2000 | Substantially Equivalent |
| K000441 | BODYGUARD | Apr 11, 2000 | Substantially Equivalent |
| K994044 | CLEEN-ABLE | Feb 25, 2000 | Substantially Equivalent |
| K990412 | CUFF-ABLE PLUS | Sep 1, 1999 | Substantially Equivalent |