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FDA 510(k)

MASH DERMATOME

K-Number: K861138 · 1986-04-14

ApplicantMecron Medical Products, Inc.
Decision Date1986-04-14
Product CodeGFD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MASH DERMATOME is the device name listed in this FDA 510(k) record. The listed applicant is Mecron Medical Products, Inc.. It received FDA 510(k) clearance on 1986-04-14 under 510(k) number K861138. 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 MASH DERMATOME?

MASH DERMATOME is a medical device that received FDA 510(k) clearance on 1986-04-14. The listed applicant is Mecron Medical Products, Inc.. The 510(k) number is K861138.

When did MASH DERMATOME receive FDA 510(k) clearance?

MASH DERMATOME received FDA 510(k) clearance on 1986-04-14, under 510(k) number K861138.

Who is the listed applicant for MASH DERMATOME?

The FDA 510(k) record lists Mecron Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MASH DERMATOME?

The FDA product code for MASH DERMATOME is GFD.

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Other records listing Mecron Medical Products, Inc. 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.

K854191MECRON UNCEMENTED STRUCTURED STEM HIPK844775EFFNER-EYE CAUTERY WITH BATTERY HANDLEK844774EFFNER FIBER OPTIC CABLES FOR COLD LIGHT TRANSMISSK844488MECRON CEMENTED STRUCTURED STEM HIP PROSTHESISK844486MECRON MRC-HEADLESS FEMORAL COMPONENTK844487MECRON FEMORAL HEAD W/CONE AS UNIPOLAR OR BIPOLAR

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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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