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FDA 510(k)

MENS FREEDOM MICRO

K-Number: K904430 · 1991-05-13

ApplicantMonad Corp.
Decision Date1991-05-13
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

MENS FREEDOM MICRO is the device name listed in this FDA 510(k) record. The listed applicant is Monad Corp.. It received FDA 510(k) clearance on 1991-05-13 under 510(k) number K904430. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MENS FREEDOM MICRO?

MENS FREEDOM MICRO is a medical device that received FDA 510(k) clearance on 1991-05-13. The listed applicant is Monad Corp.. The 510(k) number is K904430.

When did MENS FREEDOM MICRO receive FDA 510(k) clearance?

MENS FREEDOM MICRO received FDA 510(k) clearance on 1991-05-13, under 510(k) number K904430.

Who is the listed applicant for MENS FREEDOM MICRO?

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

What is the FDA product code for MENS FREEDOM MICRO?

The FDA product code for MENS FREEDOM MICRO is GZJ.

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Other records listing Monad Corp. as applicant

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.

K914441MENS 2000-DK902226MY-O-MATIC 5000IK904258MICRO DERMK904235MENS-O-MATIC 2000K904260MENS-O-MATIC 3000K904288MENS-O-MATIC 1XS AND MENS-O-MATIC 2XS

View all 9 devices →

Related Devices (Code: GZJ)

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.

K252712STIMPOD NMS460 Nerve StimulatorAlgiamed Technologies USA, Inc.K252767actiTENS miniSublimedK252236CP Relief Wand Rx - TENS/NMESN & C Holdings, LLCK232441Unipro (K-UNIPRO-US)Tenscare, Ltd.K241228TENSWaveZynex Medical OfficerK233046Electrical Neuromuscular Stimulator, Cure TrioOriental Inspiration Limited

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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