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FDA 510(k)

MINI-DIAMOND KNIFE

K-Number: K893033 · 1989-05-26

ApplicantL.A.B. Instruments
Decision Date1989-05-26
Product CodeGDX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MINI-DIAMOND KNIFE is the device name listed in this FDA 510(k) record. The listed applicant is L.A.B. Instruments. It received FDA 510(k) clearance on 1989-05-26 under 510(k) number K893033. The device is classified under product code GDX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINI-DIAMOND KNIFE?

MINI-DIAMOND KNIFE is a medical device that received FDA 510(k) clearance on 1989-05-26. The listed applicant is L.A.B. Instruments. The 510(k) number is K893033.

When did MINI-DIAMOND KNIFE receive FDA 510(k) clearance?

MINI-DIAMOND KNIFE received FDA 510(k) clearance on 1989-05-26, under 510(k) number K893033.

Who is the listed applicant for MINI-DIAMOND KNIFE?

The FDA 510(k) record lists L.A.B. Instruments as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MINI-DIAMOND KNIFE?

The FDA product code for MINI-DIAMOND KNIFE is GDX.

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Related Devices (Code: GDX)

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.

K923689SURGISTAR BLADESSurgistar, Inc.K921167ULTRABLADEMicron Technology, Inc.K914086ICAN CYLINDRICAL SPONGESIcn Pharmaceuticals, Inc.K904505CCI CORNEAL SCARIFIERBuckman Co., Inc.K9053801-CUT ACL GRAFT KNIFEDepuy, Inc.K895682VESSEL LOOPSApplied Medical Technologies

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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