ELECTROSURGICAL COAGULATION SUCTION TUBE— 510(k) K895337

Name: FDA 510(k) clearance K895337
Creator: U.S. Food and Drug Administration
Published: 1989-09-15

Substantially Equivalent

New England Surgical Instrument Corp.

FDA 510(k) clearance K895337 for ELECTROSURGICAL COAGULATION SUCTION TUBE, Substantially Equivalent on 1989-09-15. Applicant: New England Surgical Instrument Corp.. Device class: 2.

Clearance details

Applicant: New England Surgical Instrument Corp.
Product code: Code HAM
Device class: Class 2
Regulation: 21 CFR 878.4400
Advisory panel: General, Plastic Surgery
Date received: 1989-08-30
Decision date: 1989-09-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rockland, MA, US

Download summary PDF View on FDA.gov ↗

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