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.

Clearance details

Applicant
Medsonics
Product code
Code JOM
Advisory panel
Cardiovascular
Date received
Decision date
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.