MONITOR, CARDIAC, W/BLOOD PRESS.&TEMP— 510(k) K772334

Name: FDA 510(k) clearance K772334
Creator: U.S. Food and Drug Administration
Published: 1978-02-21

Substantially Equivalent

Telectronics, Inc.

FDA 510(k) clearance K772334 for MONITOR, CARDIAC, W/BLOOD PRESS.&TEMP, Substantially Equivalent on 1978-02-21. Applicant: Telectronics, Inc.. Device class: 2.

Clearance details

Applicant: Telectronics, Inc.
Product code: Code DSK
Device class: Class 2
Regulation: 21 CFR 870.1110
Advisory panel: Cardiovascular
Date received: 1977-12-22
Decision date: 1978-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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