MODEL V420 DIRECT PRESSURE MONITOR & 427 WAVEFORM— 510(k) K893232

Name: FDA 510(k) clearance K893232
Creator: U.S. Food and Drug Administration
Published: 1989-07-14

Substantially Equivalent

Camino Laboratories, Inc.

FDA 510(k) clearance K893232 for MODEL V420 DIRECT PRESSURE MONITOR & 427 WAVEFORM, Substantially Equivalent on 1989-07-14. Applicant: Camino Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Camino Laboratories, Inc.
Product code: Code DSK
Device class: Class 2
Regulation: 21 CFR 870.1110
Advisory panel: Cardiovascular
Date received: 1989-04-28
Decision date: 1989-07-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

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