THERAPEUTIC APPARATUS, DIERKER TYPE— 510(k) K770534

Name: FDA 510(k) clearance K770534
Creator: U.S. Food and Drug Administration
Published: 1978-04-21

Substantially Equivalent

Well Being Ent.

FDA 510(k) clearance K770534 for THERAPEUTIC APPARATUS, DIERKER TYPE, Substantially Equivalent on 1978-04-21. Applicant: Well Being Ent.. Device class: 2.

Clearance details

Applicant: Well Being Ent.
Product code: Code KDH
Device class: Class 2
Regulation: 21 CFR 876.5980
Advisory panel: Gastroenterology, Urology
Date received: 1977-03-21
Decision date: 1978-04-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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