meddevicedb.com FDA Device Reference

WHATMAN BODY FLUID COLLECTION PAPER:WHATMAN BFC180

K932661 Class II Traditional
Decision Date
1996-04-17
Sponsor / Applicant
Whatman Specialty Products, Inc.

Technical Specification

510(k) Submission ID K932661
Product Code PJC
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1675
Decision Date 1996-04-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

WHATMAN BODY FLUID COLLECTION PAPER:WHATMAN BFC180 received FDA 510(k) clearance under submission number K932661, sponsored by Whatman Specialty Products, Inc.. 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 1996-04-17.

Classification & Regulation

This clearance is catalogued under FDA product code PJC and 21 CFR 862.1675, within the Clinical Chemistry review panel as a Class II device.