4600 RECORDER— 510(k) K780677

Name: FDA 510(k) clearance K780677
Creator: U.S. Food and Drug Administration
Published: 1978-05-17

Substantially Equivalent

G & W Applied Science Laboratories

FDA 510(k) clearance K780677 for 4600 RECORDER, Substantially Equivalent on 1978-05-17. Applicant: G & W Applied Science Laboratories. Device class: 1.

Clearance details

Applicant: G & W Applied Science Laboratories
Product code: Code DSF
Device class: Class 1
Regulation: 21 CFR 870.2810
Advisory panel: Cardiovascular
Date received: 1978-04-24
Decision date: 1978-05-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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