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FDA 510(k)

SUPERSKIN

K-Number: K972081 · 1997-12-17

ApplicantMedlogic Global Corp.
Decision Date1997-12-17
Product CodeNEC
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SUPERSKIN is the device name listed in this FDA 510(k) record. The listed applicant is Medlogic Global Corp.. It received FDA 510(k) clearance on 1997-12-17 under 510(k) number K972081. The device is classified under product code NEC. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUPERSKIN?

SUPERSKIN is a medical device that received FDA 510(k) clearance on 1997-12-17. The listed applicant is Medlogic Global Corp.. The 510(k) number is K972081.

When did SUPERSKIN receive FDA 510(k) clearance?

SUPERSKIN received FDA 510(k) clearance on 1997-12-17, under 510(k) number K972081.

Who is the listed applicant for SUPERSKIN?

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

What is the FDA product code for SUPERSKIN?

The FDA product code for SUPERSKIN is NEC.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Medlogic Global 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.

K993556LIQUIBAND DENTAL

Related Devices (Code: NEC)

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.

K861557APLICARE SKIN PROTECTANT PREP PADAplicare, Inc.K861558APLICARE SKIN PROTECTANT SWABSTICKAplicare, Inc.

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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