PATIENT MOVER(TM)— 510(k) K890555

Substantially Equivalent

T.B.S., Inc.

FDA 510(k) clearance K890555 for PATIENT MOVER(TM), Substantially Equivalent on 1989-02-13. Applicant: T.B.S., Inc.. Device class: 2.

Clearance details

Applicant: T.B.S., Inc.
Product code: Code ILK
Device class: Class 2
Regulation: 21 CFR 890.5150
Advisory panel: Physical Medicine
Date received: 1989-02-06
Decision date: 1989-02-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ventura, CA, US

Download summary PDF View on FDA.gov ↗

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More clearances from T.B.S., Inc.

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