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FDA 510(k)

ZEISS OPERATING KERATOMETER

K-Number: K853723 · 1985-10-15

ApplicantCarl Zeiss, Inc.
Decision Date1985-10-15
Product CodeHLQ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ZEISS OPERATING KERATOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Carl Zeiss, Inc.. It received FDA 510(k) clearance on 1985-10-15 under 510(k) number K853723. The device is classified under product code HLQ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZEISS OPERATING KERATOMETER?

ZEISS OPERATING KERATOMETER is a medical device that received FDA 510(k) clearance on 1985-10-15. The listed applicant is Carl Zeiss, Inc.. The 510(k) number is K853723.

When did ZEISS OPERATING KERATOMETER receive FDA 510(k) clearance?

ZEISS OPERATING KERATOMETER received FDA 510(k) clearance on 1985-10-15, under 510(k) number K853723.

Who is the listed applicant for ZEISS OPERATING KERATOMETER?

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

What is the FDA product code for ZEISS OPERATING KERATOMETER?

The FDA product code for ZEISS OPERATING KERATOMETER is HLQ.

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Other records listing Carl Zeiss, Inc. as applicant

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Related Devices (Code: HLQ)

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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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