PROTOUCH OVERGLOVE— 510(k) K952241

Substantially Equivalent

Cottrell, Ltd.

FDA 510(k) clearance K952241 for PROTOUCH OVERGLOVE, Substantially Equivalent on 1995-08-07. Applicant: Cottrell, Ltd.. Device class: 2.

Clearance details

Applicant: Cottrell, Ltd.
Product code: Code MMP
Device class: Class 2
Regulation: 21 CFR 878.4370
Advisory panel: General, Plastic Surgery
Date received: 1995-05-12
Decision date: 1995-08-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: North Attleboro, MA, US

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