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FDA 510(k)

CILCO DIAMOND KNIFE

K-Number: K843447 · 1984-10-05

ApplicantCilco, Inc.
Decision Date1984-10-05
Product CodeHNN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CILCO DIAMOND KNIFE is the device name listed in this FDA 510(k) record. The listed applicant is Cilco, Inc.. It received FDA 510(k) clearance on 1984-10-05 under 510(k) number K843447. The device is classified under product code HNN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CILCO DIAMOND KNIFE?

CILCO DIAMOND KNIFE is a medical device that received FDA 510(k) clearance on 1984-10-05. The listed applicant is Cilco, Inc.. The 510(k) number is K843447.

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

CILCO DIAMOND KNIFE received FDA 510(k) clearance on 1984-10-05, under 510(k) number K843447.

Who is the listed applicant for CILCO DIAMOND KNIFE?

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

What is the FDA product code for CILCO DIAMOND KNIFE?

The FDA product code for CILCO DIAMOND KNIFE is HNN.

Related Clinical Trials

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.

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Other records listing Cilco, 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.

K861334CILCO DIAMOND KNIVES & DIAMOND KNIFE LINEAR GAUGEK854969CILCO SONOMETRICS A&B DIGITAL SYSTEM (DIGISCAN)K844249K-SOLK843319CILCO I/A SURGICAL PACKK843992CILCOR OPHTHALMIC INSTRUMENTSK841099OCTOPUS 500/500E

View all 12 devices →

Related Devices (Code: HNN)

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.

K110166CLEARCUT S SAFETY KNIFEAlcon Research, Ltd.K922378OPHTHALMIC KNIFEMicroptics Development LaboratoryK882402RETRACTIVE INCISION MICROMETER (RIM) GUAGEOptical CenterK881669MVR/STILETTO BLADE 20GA. - P/N 1900Advanced Surgical Products, Inc.K874979PRISMA DISPOSABLE MVR/STILETTO BLADEAdvanced Surgical Products, Inc.K874057OPHTHALMIC TIP & BLADE SCALPELSMyocure, 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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