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FDA 510(k)

EXERCISER, RESP., DEEP BREATHING

K-Number: K780037 · 1978-02-24

ApplicantMedical Technologies of Georgia
Decision Date1978-02-24
Product CodeBWF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

EXERCISER, RESP., DEEP BREATHING is the device name listed in this FDA 510(k) record. The listed applicant is Medical Technologies of Georgia. It received FDA 510(k) clearance on 1978-02-24 under 510(k) number K780037. The device is classified under product code BWF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXERCISER, RESP., DEEP BREATHING?

EXERCISER, RESP., DEEP BREATHING is a medical device that received FDA 510(k) clearance on 1978-02-24. The listed applicant is Medical Technologies of Georgia. The 510(k) number is K780037.

When did EXERCISER, RESP., DEEP BREATHING receive FDA 510(k) clearance?

EXERCISER, RESP., DEEP BREATHING received FDA 510(k) clearance on 1978-02-24, under 510(k) number K780037.

Who is the listed applicant for EXERCISER, RESP., DEEP BREATHING?

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

What is the FDA product code for EXERCISER, RESP., DEEP BREATHING?

The FDA product code for EXERCISER, RESP., DEEP BREATHING is BWF.

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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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