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FDA 510(k)

MICRO DERM

K-Number: K904258 · 1991-05-13

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

Device Summary

MICRO DERM 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 K904258. 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 MICRO DERM?

MICRO DERM 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 K904258.

When did MICRO DERM receive FDA 510(k) clearance?

MICRO DERM received FDA 510(k) clearance on 1991-05-13, under 510(k) number K904258.

Who is the listed applicant for MICRO DERM?

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 MICRO DERM?

The FDA product code for MICRO DERM 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 5000IK904235MENS-O-MATIC 2000K904260MENS-O-MATIC 3000K904430MENS FREEDOM MICROK904288MENS-O-MATIC 1XS AND MENS-O-MATIC 2XS

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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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