ROCKET INTRAUTERINE SOUND— 510(k) K883806

Substantially Equivalent

A & A Medical, Inc.

FDA 510(k) clearance K883806 for ROCKET INTRAUTERINE SOUND, Substantially Equivalent on 1988-10-31. Applicant: A & A Medical, Inc.. Device class: 1.

Clearance details

Applicant: A & A Medical, Inc.
Product code: Code HHM
Device class: Class 1
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 1988-09-07
Decision date: 1988-10-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Branford, CT, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HHM

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K840380 — UTERINE SOUND1984-04-30

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