510(k) K901508
K901508 is an FDA 510(k) premarket notification submitted by Retrax, Inc. for the device "RETRAX SAFETY SYRINGE". The FDA issued a decision of Substantially Equivalent on June 14, 1990. The device falls under product code FMF (Syringe, Piston), a Class II device regulated under 21 CFR 880.5860. Retrax, Inc. has at least 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- June 14, 1990
- Date Received
- March 30, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Syringe, Piston
- Device Class
- Class II
- Regulation Number
- 880.5860
- Review Panel
- HO
- Submission Type