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FDA 510(k)

PILLING DIAMOND KNIFE

K-Number: K822749 · 1982-10-06

ApplicantNarco Scientific
Decision Date1982-10-06
Product CodeGDX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PILLING DIAMOND KNIFE is the device name listed in this FDA 510(k) record. The listed applicant is Narco Scientific. It received FDA 510(k) clearance on 1982-10-06 under 510(k) number K822749. 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 PILLING DIAMOND KNIFE?

PILLING DIAMOND KNIFE is a medical device that received FDA 510(k) clearance on 1982-10-06. The listed applicant is Narco Scientific. The 510(k) number is K822749.

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

PILLING DIAMOND KNIFE received FDA 510(k) clearance on 1982-10-06, under 510(k) number K822749.

Who is the listed applicant for PILLING DIAMOND KNIFE?

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

What is the FDA product code for PILLING DIAMOND KNIFE?

The FDA product code for PILLING DIAMOND KNIFE is GDX.

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Other records listing Narco Scientific 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.

K830338NARCOTRACE 80K831429AS 191 ECG TELEMETRY MODULEK831428AS 1740 INTERFACE MODULEK822835PZ-800 VOLUME VENTILATORK831430AIR SHIELDS AS-100 MONIORING SYS-AS105K831460AS 30/TCP MODULE

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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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