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FDA 510(k)

TERRY KERATOMETER

K-Number: K781650 · 1978-10-17

ApplicantClifford M. Terry, M.C.
Decision Date1978-10-17
Product CodeHJA
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

TERRY KERATOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Clifford M. Terry, M.C.. It received FDA 510(k) clearance on 1978-10-17 under 510(k) number K781650. The device is classified under product code HJA. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TERRY KERATOMETER?

TERRY KERATOMETER is a medical device that received FDA 510(k) clearance on 1978-10-17. The listed applicant is Clifford M. Terry, M.C.. The 510(k) number is K781650.

When did TERRY KERATOMETER receive FDA 510(k) clearance?

TERRY KERATOMETER received FDA 510(k) clearance on 1978-10-17, under 510(k) number K781650.

Who is the listed applicant for TERRY KERATOMETER?

The FDA 510(k) record lists Clifford M. Terry, M.C. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TERRY KERATOMETER?

The FDA product code for TERRY KERATOMETER is HJA.

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Related Devices (Code: HJA)

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.

K901523VKG 1000, VIDEO KERATOGRAPHThe Sanborn Co.K893968VKG 2000 VIDEO KERATOMETERTechnitex, Inc.K842128AMERICAN MEDICAL OPTICS PHOTOKERATOAmerican Medical OpticsK830290DORC CONTACT/PHOTO DERATOSCOPEJedmed Instrument Co.

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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