meddevicedb.com FDA Device Reference

QUICK PRIME LINES, #'S BPL-12, BPL-48 &

K802378 Class II Traditional
Decision Date
1980-10-10
Sponsor / Applicant
Bentley Laboratories, Inc.

Technical Specification

510(k) Submission ID K802378
Product Code DWF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4210
Decision Date 1980-10-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QUICK PRIME LINES, #'S BPL-12, BPL-48 & received FDA 510(k) clearance under submission number K802378, sponsored by Bentley Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1980-10-10.

Classification & Regulation

This clearance is catalogued under FDA product code DWF and 21 CFR 870.4210, within the Cardiovascular review panel as a Class II device.