ENDOPORT EROCAR— 510(k) K841716

Substantially Equivalent

Endotherapeutics

FDA 510(k) clearance K841716 for ENDOPORT EROCAR, Substantially Equivalent on 1984-06-28. Applicant: Endotherapeutics. Device class: 2.

Clearance details

Applicant: Endotherapeutics
Product code: Code FBQ
Device class: Class 2
Regulation: 21 CFR 876.5090
Advisory panel: Gastroenterology, Urology
Date received: 1984-04-25
Decision date: 1984-06-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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More clearances from Endotherapeutics

K870855 — UROSCAN1987-06-09
K860192 — ENDOPORT 5MM SINGLE-USE TROCAR AND SLEEVE1986-03-17
K860102 — MOD. ENDONEEDLE SINGLE-USE PNEUMOPERITONEUM NEEDLE1986-02-12
K860103 — MOD. ENDOPORT SINGLE-USE TROCAR AND SLEEVE1986-02-12
K852031 — ENDOPORT 5MM1985-08-13

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