DANTEC MENUET— 510(k) K896575

Substantially Equivalent

Dantec Medical, Inc.

FDA 510(k) clearance K896575 for DANTEC MENUET, Substantially Equivalent on 1990-05-03. Applicant: Dantec Medical, Inc.. Device class: 2.

Clearance details

Applicant: Dantec Medical, Inc.
Product code: Code FAP
Device class: Class 2
Regulation: 21 CFR 876.1620
Advisory panel: Gastroenterology, Urology
Date received: 1989-11-20
Decision date: 1990-05-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mahwah, NJ, US

Download summary PDF View on FDA.gov ↗

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More clearances from Dantec Medical, Inc.

K960503 — DANTEC DUET1996-09-16
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K953999 — DANTEC DA CAPO1995-11-21
K926363 — MULTI-DOP S1995-06-19
K931801 — MULTI-DOP X1995-06-14

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