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BIOSURGICAL, CORP. MULTI CHAMBER SUCTION SYRINGE

K964597 Class II Traditional
Decision Date
1997-09-08
Sponsor / Applicant
Biosurgical Corp.

Technical Specification

510(k) Submission ID K964597
Product Code FMF
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5860
Decision Date 1997-09-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIOSURGICAL, CORP. MULTI CHAMBER SUCTION SYRINGE received FDA 510(k) clearance under submission number K964597, sponsored by Biosurgical Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1997-09-08.

Classification & Regulation

This clearance is catalogued under FDA product code FMF and 21 CFR 880.5860, within the General Hospital review panel as a Class II device.