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FDA 510(k)

MERCURY MEDICAL EXPIRATORY RESISTANCE EXERCISER, RESISTEX

K-Number: K954492 · 1996-10-21

ApplicantMercury Medical
Decision Date1996-10-21
Product CodeBWF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MERCURY MEDICAL EXPIRATORY RESISTANCE EXERCISER, RESISTEX is the device name listed in this FDA 510(k) record. The listed applicant is Mercury Medical. It received FDA 510(k) clearance on 1996-10-21 under 510(k) number K954492. 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 MEDICAL EXPIRATORY RESISTANCE EXERCISER, RESISTEX?

MERCURY MEDICAL EXPIRATORY RESISTANCE EXERCISER, RESISTEX is a medical device that received FDA 510(k) clearance on 1996-10-21. The listed applicant is Mercury Medical. The 510(k) number is K954492.

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

MERCURY MEDICAL EXPIRATORY RESISTANCE EXERCISER, RESISTEX received FDA 510(k) clearance on 1996-10-21, under 510(k) number K954492.

Who is the listed applicant for MERCURY MEDICAL EXPIRATORY RESISTANCE EXERCISER, RESISTEX?

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

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

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

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Other records listing Mercury Medical as applicant

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Related Devices (Code: BWF)

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.

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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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