510(k) K883008
K883008 is an FDA 510(k) premarket notification submitted by Medical Associated Services, Inc. for the device "PULMONARY FORCED FLOW SYSTEM (PUFFS)". The FDA issued a decision of Substantially Equivalent on September 29, 1988. The device falls under product code BTY (Calculator, Predicted Values, Pulmonary Function), a Class II device regulated under 21 CFR 868.1890. Medical Associated Services, Inc. has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 29, 1988
- Date Received
- July 18, 1988
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Calculator, Predicted Values, Pulmonary Function
- Device Class
- Class II
- Regulation Number
- 868.1890
- Review Panel
- AN
- Submission Type