510(k) K760031
K760031 is an FDA 510(k) premarket notification submitted by Harleco for the device "HISTOCHEMICAL PAS REACTION SET". The FDA issued a decision of Substantially Equivalent on July 20, 1976. The device falls under product code HZT (Reagent, Schiff), a Class I device regulated under 21 CFR 864.1850. Harleco has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 20, 1976
- Date Received
- June 14, 1976
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Reagent, Schiff
- Device Class
- Class I
- Regulation Number
- 864.1850
- Review Panel
- PA
- Submission Type