510(k) K910680
K910680 is an FDA 510(k) premarket notification submitted by Helena Laboratories for the device "EPINEPHRINE REAGENT, CAT. NO. 5367". The FDA issued a decision of Substantially Equivalent on May 20, 1991. The device falls under product code GHR (Reagent, Platelet Aggregation), a Class II device regulated under 21 CFR 864.5700. Helena Laboratories has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 20, 1991
- Date Received
- February 15, 1991
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Reagent, Platelet Aggregation
- Device Class
- Class II
- Regulation Number
- 864.5700
- Review Panel
- HE
- Submission Type