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FDA 510(k)

CILCO I/A HANDPIECE

K-Number: K820933 · 1982-06-14

ApplicantCilco, Inc.
Decision Date1982-06-14
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CILCO I/A HANDPIECE is the device name listed in this FDA 510(k) record. The listed applicant is Cilco, Inc.. It received FDA 510(k) clearance on 1982-06-14 under 510(k) number K820933. The device is classified under product code HQE. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CILCO I/A HANDPIECE?

CILCO I/A HANDPIECE is a medical device that received FDA 510(k) clearance on 1982-06-14. The listed applicant is Cilco, Inc.. The 510(k) number is K820933.

When did CILCO I/A HANDPIECE receive FDA 510(k) clearance?

CILCO I/A HANDPIECE received FDA 510(k) clearance on 1982-06-14, under 510(k) number K820933.

Who is the listed applicant for CILCO I/A HANDPIECE?

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 I/A HANDPIECE?

The FDA product code for CILCO I/A HANDPIECE is HQE.

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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 INSTRUMENTSK843447CILCO DIAMOND KNIFE

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Related Devices (Code: HQE)

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.

K212763UniVit HE, UniVit UHSVisioncare Devices, LLCK170183Cetus system, Cetus probeA.R.C Laser GmbHK153168Bi-Blade Vitrectomy CutterMedical Instrument Development LaboratoriesK121675VERSAVITSynergetics, Inc.K120170PROCARE PLUS VITRECTOMY SYSTEMVisioncare Devices, Inc.K102222ULTIMATE VIT ENHAMCER (UVE)Medical Instrument Development Laboratories, 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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