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PLATELET EXTRACT REAGENT

K873382 Class II Traditional
Decision Date
1987-11-20
Sponsor / Applicant
Bio/Data Corp.

Technical Specification

510(k) Submission ID K873382
Product Code GGW
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7925
Decision Date 1987-11-20
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PLATELET EXTRACT REAGENT received FDA 510(k) clearance under submission number K873382, sponsored by Bio/Data Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 1987-11-20.

Classification & Regulation

This clearance is catalogued under FDA product code GGW and 21 CFR 864.7925, within the Hematology review panel as a Class II device.