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FDA 510(k)

CILCO VILLASENOR PACHYMETER

K-Number: K882805 · 1988-08-12

ApplicantCoopervision-Cilco
Decision Date1988-08-12
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CILCO VILLASENOR PACHYMETER is the device name listed in this FDA 510(k) record. The listed applicant is Coopervision-Cilco. It received FDA 510(k) clearance on 1988-08-12 under 510(k) number K882805. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CILCO VILLASENOR PACHYMETER?

CILCO VILLASENOR PACHYMETER is a medical device that received FDA 510(k) clearance on 1988-08-12. The listed applicant is Coopervision-Cilco. The 510(k) number is K882805.

When did CILCO VILLASENOR PACHYMETER receive FDA 510(k) clearance?

CILCO VILLASENOR PACHYMETER received FDA 510(k) clearance on 1988-08-12, under 510(k) number K882805.

Who is the listed applicant for CILCO VILLASENOR PACHYMETER?

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

What is the FDA product code for CILCO VILLASENOR PACHYMETER?

The FDA product code for CILCO VILLASENOR PACHYMETER is IYO.

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 Coopervision-Cilco 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.

K883489KRATZ NOVA SERT(TM)

Related Devices (Code: IYO)

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.

K260313MD-6000S Bladder ScannerMEDA Co., Ltd.K253452Accuro 3SRivanna Medical, Inc.K260190ARTHURROPCA ApSK252237EdgeFlow UW20Edgecare, Inc.K254021Accuro XVRivanna Medical, Inc.K253898QT Scanner 2000 Model AQT Imaging Holdings, 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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