FDA 510(k)
FDA class 2
Substantially Equivalent
🇺🇸 United States
MERCURY RHINOMANOMETER
K Number: K902120
·
Decision Aug 6, 1990
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
11
Applicant Total
68
Review Days
87
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Basic Information
- Device Name
- MERCURY RHINOMANOMETER
- K Number
- K902120
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 868.1800
- Medical Specialty
- Anesthesiology
- Decision
- Substantially Equivalent
- Applicant
- Life-Tech Intl., Inc.
- Date Received
- May 11, 1990
- Decision Date
- August 6, 1990
- Product Code
- BXQ
- Advisory Committee
- Anesthesiology
- Review Advisory Committee
- AN
- 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 |
|---|---|---|---|
| BXQ | Rhinoanemometer (Measurement Of Nasal Decongestion) | FDA class 2 | Anesthesiology |
Similar 510(k) Clearances
Other 510(k) clearances with the same product code (BXQ), ordered by most recent decision date.
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| K954315 | PVC ABDOMINAL/RECTAL PRESSURE CATHETER | Nov 30, 1995 | Substantially Equivalent |
| K954341 | URODYNAMICS TUBING AND INFUSION SETS | Oct 17, 1995 | Substantially Equivalent |
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| K953353 | UROVISION JANUS | Sep 8, 1995 | Substantially Equivalent |
| K946108 | EAR-A-GATOR | Jun 13, 1995 | Substantially Equivalent |
| K913601 | MICROPHOR | Jul 15, 1994 | Substantially Equivalent |
| K940203 | TRIPLE LUMEN URODYNAMIC CATHETER WITH RADIOPAQUE MARKERS | Mar 30, 1994 | Substantially Equivalent |