CABOT MEDICAL IRRIGATION FLUID WARMER SETS— 510(k) K932538

Name: FDA 510(k) clearance K932538
Creator: U.S. Food and Drug Administration
Published: 1994-02-22

Substantially Equivalent

Cabot Medical Corp.

FDA 510(k) clearance K932538 for CABOT MEDICAL IRRIGATION FLUID WARMER SETS, Substantially Equivalent on 1994-02-22. Applicant: Cabot Medical Corp.. Device class: 1.

Clearance details

Applicant: Cabot Medical Corp.
Product code: Code LHC
Device class: Class 1
Regulation: 21 CFR 890.5950
Advisory panel: Physical Medicine
Date received: 1993-05-26
Decision date: 1994-02-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Langhorne, PA, US

Download summary PDF View on FDA.gov ↗

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K142080 — NON-STERILE ORS WARNING DRAPES/SLUSH+WARMER DISC-DRAPE/SLUSH+WARMER PALTE-DRAPE /FLUID WARMER DRAPE,SKIRTED2014-08-28

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