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FDA 510(k)

BT-795/ATS

K-Number: K871847 · 1987-06-19

Decision Date1987-06-19
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BT-795/ATS is the device name listed in this FDA 510(k) record. The listed applicant is Electromedics, Inc.. It received FDA 510(k) clearance on 1987-06-19 under 510(k) number K871847. The device is classified under product code CAC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BT-795/ATS?

BT-795/ATS is a medical device that received FDA 510(k) clearance on 1987-06-19. The listed applicant is Electromedics, Inc.. The 510(k) number is K871847.

When did BT-795/ATS receive FDA 510(k) clearance?

BT-795/ATS received FDA 510(k) clearance on 1987-06-19, under 510(k) number K871847.

Who is the listed applicant for BT-795/ATS?

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

What is the FDA product code for BT-795/ATS?

The FDA product code for BT-795/ATS is CAC.

Other records listing Electromedics, 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.

View all 41 devices →

Related Devices (Code: CAC)

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

View on FDA Database →

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

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