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FDA 510(k)

SKIN MESH DEVICE

K-Number: K861285 · 1986-04-17

ApplicantPrecision Modified Devices
Decision Date1986-04-17
Product CodeGFD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SKIN MESH DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Precision Modified Devices. It received FDA 510(k) clearance on 1986-04-17 under 510(k) number K861285. 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 SKIN MESH DEVICE?

SKIN MESH DEVICE is a medical device that received FDA 510(k) clearance on 1986-04-17. The listed applicant is Precision Modified Devices. The 510(k) number is K861285.

When did SKIN MESH DEVICE receive FDA 510(k) clearance?

SKIN MESH DEVICE received FDA 510(k) clearance on 1986-04-17, under 510(k) number K861285.

Who is the listed applicant for SKIN MESH DEVICE?

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

What is the FDA product code for SKIN MESH DEVICE?

The FDA product code for SKIN MESH DEVICE is GFD.

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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.

K965256DMS-1000C DERMOABRADERMattioli Engineering, SrlK962371DERMTOME 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.

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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