AMPLIFIER, PHOTOPULSE, MODEL PA13— 510(k) K770332

Substantially Equivalent

Medsonics

FDA 510(k) clearance K770332 for AMPLIFIER, PHOTOPULSE, MODEL PA13, Substantially Equivalent on 1977-02-24. Applicant: Medsonics. Device class: 2.

Clearance details

Applicant: Medsonics
Product code: Code JOM
Device class: Class 2
Regulation: 21 CFR 870.2780
Advisory panel: Cardiovascular
Date received: 1977-02-17
Decision date: 1977-02-24
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.