A-V RECORDER— 510(k) K873041

Substantially Equivalent

Life Sciences Manufacturing, Inc.

FDA 510(k) clearance K873041 for A-V RECORDER, Substantially Equivalent on 1988-02-04. Applicant: Life Sciences Manufacturing, Inc..

Clearance details

Applicant: Life Sciences Manufacturing, Inc.
Product code: Code DPT
Advisory panel: Cardiovascular
Date received: 1987-08-04
Decision date: 1988-02-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Lebanon, NH, US

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