HORIZON 2110/HORIZON 2210 264-XXX-XXX/261-XXX-XXX— 510(k) K893133

Substantially Equivalent

Mennen Medical, Inc.

FDA 510(k) clearance K893133 for HORIZON 2110/HORIZON 2210 264-XXX-XXX/261-XXX-XXX, Substantially Equivalent on 1989-07-14. Applicant: Mennen Medical, Inc.. Device class: 2.

Clearance details

Applicant: Mennen Medical, Inc.
Product code: Code KLK
Device class: Class 2
Regulation: 21 CFR 868.2500
Advisory panel: Anesthesiology
Date received: 1989-04-25
Decision date: 1989-07-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Clarence, NY, US

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