KENDALL T.E.D./SCD SEQUENTIAL COMPRESSION DEVICE— 510(k) K932835

Name: FDA 510(k) clearance K932835
Creator: U.S. Food and Drug Administration
Published: 1993-08-06

Substantially Equivalent

Kendall Healthcare Products Co. Div.Of Tyco Health

FDA 510(k) clearance K932835 for KENDALL T.E.D./SCD SEQUENTIAL COMPRESSION DEVICE, Substantially Equivalent on 1993-08-06. Applicant: Kendall Healthcare Products Co. Div.Of Tyco Health. Device class: 2.

Clearance details

Applicant: Kendall Healthcare Products Co. Div.Of Tyco Health
Product code: Code JOW
Device class: Class 2
Regulation: 21 CFR 870.5800
Advisory panel: Cardiovascular
Date received: 1993-06-10
Decision date: 1993-08-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mansfield, MA, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.