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FDA 510(k)

MONAGHAN'S TRUE VOLUME EXERCISER

K-Number: K820606 · 1982-03-23

ApplicantMonaghan Medical Corp.
Decision Date1982-03-23
Product CodeBWF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MONAGHAN'S TRUE VOLUME EXERCISER is the device name listed in this FDA 510(k) record. The listed applicant is Monaghan Medical Corp.. It received FDA 510(k) clearance on 1982-03-23 under 510(k) number K820606. 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 MONAGHAN'S TRUE VOLUME EXERCISER?

MONAGHAN'S TRUE VOLUME EXERCISER is a medical device that received FDA 510(k) clearance on 1982-03-23. The listed applicant is Monaghan Medical Corp.. The 510(k) number is K820606.

When did MONAGHAN'S TRUE VOLUME EXERCISER receive FDA 510(k) clearance?

MONAGHAN'S TRUE VOLUME EXERCISER received FDA 510(k) clearance on 1982-03-23, under 510(k) number K820606.

Who is the listed applicant for MONAGHAN'S TRUE VOLUME EXERCISER?

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

What is the FDA product code for MONAGHAN'S TRUE VOLUME EXERCISER?

The FDA product code for MONAGHAN'S TRUE VOLUME EXERCISER 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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