LASER BRONCHOSCOPE SYSTEM— 510(k) K861921

Substantially Equivalent

Pilling Co.

FDA 510(k) clearance K861921 for LASER BRONCHOSCOPE SYSTEM, Substantially Equivalent on 1986-06-02. Applicant: Pilling Co.. Device class: 2.

Clearance details

Applicant: Pilling Co.
Product code: Code LLO
Device class: Class 2
Regulation: 21 CFR 874.4500
Advisory panel: Ear, Nose, Throat
Date received: 1986-05-19
Decision date: 1986-06-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Washington, PA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Pilling Co.

K934427 — PILLING LAPAROSCOPIC INSTRUMENTATION1994-01-10
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K925198 — KAISER NO CANNULA THORACOSCOPY/LAPAROSCOPY INSTR1993-02-12
K922971 — NO-SCALPEL VASCETOMY INSTRUMENTS1992-09-23
K914015 — CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMP1991-11-21

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