ENDOPATH VERESS NEEDLE— 510(k) K910855

Substantially Equivalent

Symbiosis Corp.

FDA 510(k) clearance K910855 for ENDOPATH VERESS NEEDLE, Substantially Equivalent on 1991-04-18. Applicant: Symbiosis Corp.. Device class: 2.

Clearance details

Applicant: Symbiosis Corp.
Product code: Code FHP
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 1991-02-28
Decision date: 1991-04-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Miami Lakes, FL, US

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Recent devices under product code FHP

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K952432 — SYMBIOSIS BIPOLAR FORCEPS1995-07-05
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Data sourced from openFDA. This site is unofficial and independent of the FDA.