ROCKET CERVICAL SPATULA— 510(k) K884042

Substantially Equivalent

A & A Medical, Inc.

FDA 510(k) clearance K884042 for ROCKET CERVICAL SPATULA, Substantially Equivalent on 1988-10-07. Applicant: A & A Medical, Inc.. Device class: 2.

Clearance details

Applicant: A & A Medical, Inc.
Product code: Code HHT
Device class: Class 2
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 1988-09-26
Decision date: 1988-10-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Branford, CT, 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.