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FDA 510(k)

DMS-1000C DERMOABRADER

K-Number: K965256 · 1996-12-09

ApplicantMattioli Engineering, Srl
Decision Date1996-12-09
Product CodeGFD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DMS-1000C DERMOABRADER is the device name listed in this FDA 510(k) record. The listed applicant is Mattioli Engineering, Srl. It received FDA 510(k) clearance on 1996-12-09 under 510(k) number K965256. The device is classified under product code GFD. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DMS-1000C DERMOABRADER?

DMS-1000C DERMOABRADER is a medical device that received FDA 510(k) clearance on 1996-12-09. The listed applicant is Mattioli Engineering, Srl. The 510(k) number is K965256.

When did DMS-1000C DERMOABRADER receive FDA 510(k) clearance?

DMS-1000C DERMOABRADER received FDA 510(k) clearance on 1996-12-09, under 510(k) number K965256.

Who is the listed applicant for DMS-1000C DERMOABRADER?

The FDA 510(k) record lists Mattioli Engineering, Srl as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DMS-1000C DERMOABRADER?

The FDA product code for DMS-1000C DERMOABRADER is GFD.

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.

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Other records listing Mattioli Engineering, Srl 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.

K941838MULTIPLE CO2 LAERS

Related Devices (Code: GFD)

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.

K962371DERMTOME BLADEDsp WorldwideK945594DECA DERMATOME (MICROMOTOR SYSTEM)Depuy Intl., Ltd.K951085PADGETT AIR DERMATOME, MODEL APadgett Instruments, Inc.K940208AESCULAP ACCU-DERMATOMEAesculap, Inc.K862669ACTIVATED PARTIAL THROMBOPLASTIN TIME TESTU. S. Diagnostics, Inc.K861285SKIN MESH DEVICEPrecision Modified Devices

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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