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FDA 510(k)

MERCURY EXPIRATORY RESISTANCE EXERCISER

K-Number: K942919 · 1994-09-19

ApplicantMercury Ent., Inc. D/B/A Mercury Medical
Decision Date1994-09-19
Product CodeBWF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MERCURY EXPIRATORY RESISTANCE EXERCISER is the device name listed in this FDA 510(k) record. The listed applicant is Mercury Ent., Inc. D/B/A Mercury Medical. It received FDA 510(k) clearance on 1994-09-19 under 510(k) number K942919. 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 MERCURY EXPIRATORY RESISTANCE EXERCISER?

MERCURY EXPIRATORY RESISTANCE EXERCISER is a medical device that received FDA 510(k) clearance on 1994-09-19. The listed applicant is Mercury Ent., Inc. D/B/A Mercury Medical. The 510(k) number is K942919.

When did MERCURY EXPIRATORY RESISTANCE EXERCISER receive FDA 510(k) clearance?

MERCURY EXPIRATORY RESISTANCE EXERCISER received FDA 510(k) clearance on 1994-09-19, under 510(k) number K942919.

Who is the listed applicant for MERCURY EXPIRATORY RESISTANCE EXERCISER?

The FDA 510(k) record lists Mercury Ent., Inc. D/B/A Mercury Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MERCURY EXPIRATORY RESISTANCE EXERCISER?

The FDA product code for MERCURY EXPIRATORY RESISTANCE EXERCISER is BWF.

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Related Devices (Code: BWF)

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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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