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FDA 510(k)

DAVOL/SIMON DERMATOME

K-Number: K792332 · 1979-12-06

ApplicantDavol, Inc.
Decision Date1979-12-06
Product CodeGFD
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DAVOL/SIMON DERMATOME is the device name listed in this FDA 510(k) record. The listed applicant is Davol, Inc.. It received FDA 510(k) clearance on 1979-12-06 under 510(k) number K792332. 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 DAVOL/SIMON DERMATOME?

DAVOL/SIMON DERMATOME is a medical device that received FDA 510(k) clearance on 1979-12-06. The listed applicant is Davol, Inc.. The 510(k) number is K792332.

When did DAVOL/SIMON DERMATOME receive FDA 510(k) clearance?

DAVOL/SIMON DERMATOME received FDA 510(k) clearance on 1979-12-06, under 510(k) number K792332.

Who is the listed applicant for DAVOL/SIMON DERMATOME?

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

What is the FDA product code for DAVOL/SIMON DERMATOME?

The FDA product code for DAVOL/SIMON DERMATOME is GFD.

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Other records listing Davol, 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.

K251557Bard® Mesh; Bard® Mesh Pre-ShapedK250098Bard Soft Mesh; Bard Soft Mesh Pre-ShapedK031213AQUASENS FLUID MONITORING SYSTEMK030307DAVOL ARTHROVENT OUTFLOW TUBINGK003323COMPOSIX KUGEL MESH, MODEL 0010201,0010202,0010203,0010204,0010205K003790DAVOL X-STREAM LAPAROSCOPIC IRRIGATION SYSTEM, MODELS 5551000, 5552000, 5552001, 552002, 5552003, 5552004, 5552005

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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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