PENNINE OXYGEN LINK TUBING— 510(k) K852081

Name: FDA 510(k) clearance K852081
Creator: U.S. Food and Drug Administration
Published: 1985-06-14

Substantially Equivalent

Pennine Medical , Ltd.

FDA 510(k) clearance K852081 for PENNINE OXYGEN LINK TUBING, Substantially Equivalent on 1985-06-14. Applicant: Pennine Medical , Ltd.. Device class: 1.

Clearance details

Applicant: Pennine Medical , Ltd.
Product code: Code BYX
Device class: Class 1
Regulation: 21 CFR 868.5860
Advisory panel: Anesthesiology
Date received: 1985-05-13
Decision date: 1985-06-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Stoughton, MA, US

Download summary PDF View on FDA.gov ↗

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K854443 — O'NEIL URINARY CATHETER INTRODUCER1986-01-08
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K844874 — PENNINE LINK YANKAUERS1985-06-06
K844876 — PENNINE NELATON CATHETERS SIZES 5,6,8,10,12,14,16,1985-06-05
K852079 — PENNINE DERBY YANKAUER1985-06-03

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