ZEROID HEMORRHOIDAL DEVICE— 510(k) K944874

Substantially Equivalent

Medical Appliance Research Corp.

FDA 510(k) clearance K944874 for ZEROID HEMORRHOIDAL DEVICE, Substantially Equivalent on 1995-08-07. Applicant: Medical Appliance Research Corp..

Clearance details

Applicant: Medical Appliance Research Corp.
Product code: Code LKX
Advisory panel: Unknown
Date received: 1994-10-03
Decision date: 1995-08-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: North Miami Beach, FL, US

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