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FDA 510(k)

CILCOR OPHTHALMIC INSTRUMENTS

K-Number: K843992 · 1984-11-21

ApplicantCilco, Inc.
Decision Date1984-11-21
Product CodeHNR
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CILCOR OPHTHALMIC INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Cilco, Inc.. It received FDA 510(k) clearance on 1984-11-21 under 510(k) number K843992. The device is classified under product code HNR. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CILCOR OPHTHALMIC INSTRUMENTS?

CILCOR OPHTHALMIC INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1984-11-21. The listed applicant is Cilco, Inc.. The 510(k) number is K843992.

When did CILCOR OPHTHALMIC INSTRUMENTS receive FDA 510(k) clearance?

CILCOR OPHTHALMIC INSTRUMENTS received FDA 510(k) clearance on 1984-11-21, under 510(k) number K843992.

Who is the listed applicant for CILCOR OPHTHALMIC INSTRUMENTS?

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 CILCOR OPHTHALMIC INSTRUMENTS?

The FDA product code for CILCOR OPHTHALMIC INSTRUMENTS is HNR.

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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 PACKK843447CILCO DIAMOND KNIFEK841099OCTOPUS 500/500E

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Related Devices (Code: HNR)

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.

K022835STEPHENS DISPOSABLE FORCEPSStephens InstrumentsK895434ALCON FOLDING FORCEPSAlcon LaboratoriesK891487SOFT LENS FOLDING BLOCKWestern Medical Products, Inc.K893199PHACO-INJECTOR(TM) INTRAOCULAR LENS IMPLANT INSTRAllergan Medical OpticsK885230MCDONALD FOLDING FORCEPSAlcon LaboratoriesK881049BRADBURY INTRAOCULAR RETINAL KIT CAT #200Microline Pentax, 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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