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FDA 510(k)

SKIN BIOPSY DEVICE

K-Number: K933324 · 1994-03-31

ApplicantNhr, Inc.
Decision Date1994-03-31
Product CodeMJG
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SKIN BIOPSY DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Nhr, Inc.. It received FDA 510(k) clearance on 1994-03-31 under 510(k) number K933324. The device is classified under product code MJG. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SKIN BIOPSY DEVICE?

SKIN BIOPSY DEVICE is a medical device that received FDA 510(k) clearance on 1994-03-31. The listed applicant is Nhr, Inc.. The 510(k) number is K933324.

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

SKIN BIOPSY DEVICE received FDA 510(k) clearance on 1994-03-31, under 510(k) number K933324.

Who is the listed applicant for SKIN BIOPSY DEVICE?

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

What is the FDA product code for SKIN BIOPSY DEVICE?

The FDA product code for SKIN BIOPSY DEVICE is MJG.

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Related Devices (Code: MJG)

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.

K080674PAJUNK'S PRIMOCUT DISPOSABLE BIOPSY SYSTEMPAJUNK GmbH MedizintechnologieK070836EXICLIP EXCS-MClevex, Inc.K983647ECHO-COAT ULTRASOUND NEEDLESSts BiopolymersK955683RNS STERILE, DISPOSABLE BREAST BIOPSY/LOCALIZATION TRAYContour Fabricators of Florida, Inc.K925870SPACERBip USA, Inc.K922919DYNACYT BIOPSY ASPIRATION DEVICEBuckman Co., 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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