I-CHANNEL RECORDER— 510(k) K833000

Substantially Equivalent

Litton Medical Electronics

FDA 510(k) clearance K833000 for I-CHANNEL RECORDER, Substantially Equivalent on 1984-06-01. Applicant: Litton Medical Electronics.

Clearance details

Applicant: Litton Medical Electronics
Product code: Code DSF
Advisory panel: Cardiovascular
Date received: 1983-08-18
Decision date: 1984-06-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

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