510(k) K884385
K884385 is an FDA 510(k) premarket notification submitted by American Bioproducts Co. for the device "FIBRI-PREST/THROMBIN-PREST CONTROLS". The FDA issued a decision of Substantially Equivalent on December 28, 1988. The device falls under product code GJA (Test, Thrombin Time), a Class II device regulated under 21 CFR 864.7875. American Bioproducts Co. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- December 28, 1988
- Date Received
- October 18, 1988
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Test, Thrombin Time
- Device Class
- Class II
- Regulation Number
- 864.7875
- Review Panel
- HE
- Submission Type