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FDA 510(k)

AMPLIFIER, PHOTOPULSE, MODEL PA13

K-Number: K770332 · 1977-02-24

ApplicantMedsonics
Decision Date1977-02-24
Product CodeJOM
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AMPLIFIER, PHOTOPULSE, MODEL PA13 is the device name listed in this FDA 510(k) record. The listed applicant is Medsonics. It received FDA 510(k) clearance on 1977-02-24 under 510(k) number K770332. The device is classified under product code JOM. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMPLIFIER, PHOTOPULSE, MODEL PA13?

AMPLIFIER, PHOTOPULSE, MODEL PA13 is a medical device that received FDA 510(k) clearance on 1977-02-24. The listed applicant is Medsonics. The 510(k) number is K770332.

When did AMPLIFIER, PHOTOPULSE, MODEL PA13 receive FDA 510(k) clearance?

AMPLIFIER, PHOTOPULSE, MODEL PA13 received FDA 510(k) clearance on 1977-02-24, under 510(k) number K770332.

Who is the listed applicant for AMPLIFIER, PHOTOPULSE, MODEL PA13?

The FDA 510(k) record lists Medsonics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AMPLIFIER, PHOTOPULSE, MODEL PA13?

The FDA product code for AMPLIFIER, PHOTOPULSE, MODEL PA13 is JOM.

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Other records listing Medsonics as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K770904PROBE, BLOOD FLOW DETECTOR PLUG-INK760751CONTINUOUS WAVE DOPPLERK760728CONTINUOUS WAVE DOPPLER ULTRASOUND

Related Devices (Code: JOM)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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