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FDA 510(k)

BRAEGEN III 10-CHANNEL TRANSMITTER-

K-Number: K832304 · 1983-08-31

Decision Date1983-08-31
Product CodeGYE
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

BRAEGEN III 10-CHANNEL TRANSMITTER- is the device name listed in this FDA 510(k) record. The listed applicant is Electro-Bio-Medical Services, Inc.. It received FDA 510(k) clearance on 1983-08-31 under 510(k) number K832304. The device is classified under product code GYE. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRAEGEN III 10-CHANNEL TRANSMITTER-?

BRAEGEN III 10-CHANNEL TRANSMITTER- is a medical device that received FDA 510(k) clearance on 1983-08-31. The listed applicant is Electro-Bio-Medical Services, Inc.. The 510(k) number is K832304.

When did BRAEGEN III 10-CHANNEL TRANSMITTER- receive FDA 510(k) clearance?

BRAEGEN III 10-CHANNEL TRANSMITTER- received FDA 510(k) clearance on 1983-08-31, under 510(k) number K832304.

Who is the listed applicant for BRAEGEN III 10-CHANNEL TRANSMITTER-?

The FDA 510(k) record lists Electro-Bio-Medical Services, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BRAEGEN III 10-CHANNEL TRANSMITTER-?

The FDA product code for BRAEGEN III 10-CHANNEL TRANSMITTER- is GYE.

Related Clinical Trials

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.

Other records listing Electro-Bio-Medical Services, Inc. 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.

Related Devices (Code: GYE)

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.

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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