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FLUSHFLO-MODEL CC1-6

K761273 Class II Traditional
Decision Date
1977-01-12
Sponsor / Applicant
Bentley Laboratories, Inc.

Technical Specification

510(k) Submission ID K761273
Product Code KRA
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1210
Decision Date 1977-01-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FLUSHFLO-MODEL CC1-6 received FDA 510(k) clearance under submission number K761273, 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 1977-01-12.

Classification & Regulation

This clearance is catalogued under FDA product code KRA and 21 CFR 870.1210, within the Cardiovascular review panel as a Class II device.