510(k) K902916
K902916 is an FDA 510(k) premarket notification submitted by Precision Medical, Inc. for the device "PRECISION MEDICAL NEB BLOCK". The FDA issued a decision of Substantially Equivalent on July 23, 1990. The device falls under product code BXY (Flowmeter, Calibration, Gas), a Class I device regulated under 21 CFR 868.2350. Precision Medical, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 23, 1990
- Date Received
- July 3, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Flowmeter, Calibration, Gas
- Device Class
- Class I
- Regulation Number
- 868.2350
- Review Panel
- AN
- Submission Type