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FDA 510(k)

BRITT LENS COMPUTER

K-Number: K790694 · 1979-08-10

ApplicantBritt Corp., Inc.
Decision Date1979-08-10
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BRITT LENS COMPUTER is the device name listed in this FDA 510(k) record. The listed applicant is Britt Corp., Inc.. It received FDA 510(k) clearance on 1979-08-10 under 510(k) number K790694. 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 BRITT LENS COMPUTER?

BRITT LENS COMPUTER is a medical device that received FDA 510(k) clearance on 1979-08-10. The listed applicant is Britt Corp., Inc.. The 510(k) number is K790694.

When did BRITT LENS COMPUTER receive FDA 510(k) clearance?

BRITT LENS COMPUTER received FDA 510(k) clearance on 1979-08-10, under 510(k) number K790694.

Who is the listed applicant for BRITT LENS COMPUTER?

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

What is the FDA product code for BRITT LENS COMPUTER?

The FDA product code for BRITT LENS COMPUTER is IYO.

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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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