SURGIPRESS SURGICAL LOOP— 510(k) K843593

Substantially Equivalent

Syntex Corp.

FDA 510(k) clearance K843593 for SURGIPRESS SURGICAL LOOP, Substantially Equivalent on 1984-10-24. Applicant: Syntex Corp.. Device class: 1.

Clearance details

Applicant: Syntex Corp.
Product code: Code HRQ
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1984-09-12
Decision date: 1984-10-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Palo Alto, CA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.