meddevicedb.com FDA Device Reference

SINGLE VIAL 10 SGPT-TRIS

K780636 Class I Traditional
Decision Date
1978-05-18
Sponsor / Applicant
Boehringer Mannheim Corp.

Technical Specification

510(k) Submission ID K780636
Product Code CKA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1030
Decision Date 1978-05-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SINGLE VIAL 10 SGPT-TRIS received FDA 510(k) clearance under submission number K780636, sponsored by Boehringer Mannheim Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 1978-05-18.

Classification & Regulation

This clearance is catalogued under FDA product code CKA and 21 CFR 862.1030, within the Clinical Chemistry review panel as a Class I device.