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FDA 510(k)

BT-795/P AUTOMATED AUTOTRANS

K-Number: K860306 · 1986-03-06

ApplicantElectromedics, Inc.
Decision Date1986-03-06
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BT-795/P AUTOMATED AUTOTRANS is the device name listed in this FDA 510(k) record. The listed applicant is Electromedics, Inc.. It received FDA 510(k) clearance on 1986-03-06 under 510(k) number K860306. 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/P AUTOMATED AUTOTRANS?

BT-795/P AUTOMATED AUTOTRANS is a medical device that received FDA 510(k) clearance on 1986-03-06. The listed applicant is Electromedics, Inc.. The 510(k) number is K860306.

When did BT-795/P AUTOMATED AUTOTRANS receive FDA 510(k) clearance?

BT-795/P AUTOMATED AUTOTRANS received FDA 510(k) clearance on 1986-03-06, under 510(k) number K860306.

Who is the listed applicant for BT-795/P AUTOMATED AUTOTRANS?

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/P AUTOMATED AUTOTRANS?

The FDA product code for BT-795/P AUTOMATED AUTOTRANS is CAC.

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Related Devices (Code: CAC)

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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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