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FDA 510(k)

BRITT KRYPTON LASERS 150K & 152K

K-Number: K813492 · 1982-01-22

ApplicantBritt Corp., Inc.
Decision Date1982-01-22
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BRITT KRYPTON LASERS 150K & 152K 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 1982-01-22 under 510(k) number K813492. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRITT KRYPTON LASERS 150K & 152K?

BRITT KRYPTON LASERS 150K & 152K is a medical device that received FDA 510(k) clearance on 1982-01-22. The listed applicant is Britt Corp., Inc.. The 510(k) number is K813492.

When did BRITT KRYPTON LASERS 150K & 152K receive FDA 510(k) clearance?

BRITT KRYPTON LASERS 150K & 152K received FDA 510(k) clearance on 1982-01-22, under 510(k) number K813492.

Who is the listed applicant for BRITT KRYPTON LASERS 150K & 152K?

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 KRYPTON LASERS 150K & 152K?

The FDA product code for BRITT KRYPTON LASERS 150K & 152K is HQF.

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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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