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FDA 510(k)

CROUCH CORNEAL PROTECTOR

K-Number: K811577 · 1981-08-07

ApplicantDenver Biomedicals, Inc.
Decision Date1981-08-07
Product CodeHOY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CROUCH CORNEAL PROTECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Denver Biomedicals, Inc.. It received FDA 510(k) clearance on 1981-08-07 under 510(k) number K811577. The device is classified under product code HOY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CROUCH CORNEAL PROTECTOR?

CROUCH CORNEAL PROTECTOR is a medical device that received FDA 510(k) clearance on 1981-08-07. The listed applicant is Denver Biomedicals, Inc.. The 510(k) number is K811577.

When did CROUCH CORNEAL PROTECTOR receive FDA 510(k) clearance?

CROUCH CORNEAL PROTECTOR received FDA 510(k) clearance on 1981-08-07, under 510(k) number K811577.

Who is the listed applicant for CROUCH CORNEAL PROTECTOR?

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

What is the FDA product code for CROUCH CORNEAL PROTECTOR?

The FDA product code for CROUCH CORNEAL PROTECTOR is HOY.

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Other records listing Denver Biomedicals, Inc. as applicant

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Related Devices (Code: HOY)

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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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