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FDA 510(k)

BLUE GREEN FILTER SYSTEM TO MODEL 152 AND 150 LASER SYSTEM

K-Number: K837151 · 1983-03-22

ApplicantBritt Corp., Inc.
Decision Date1983-03-22
Product Code
DecisionSubstantially Equivalent

Device Summary

BLUE GREEN FILTER SYSTEM TO MODEL 152 AND 150 LASER SYSTEM 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 1983-03-22 under 510(k) number K837151. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BLUE GREEN FILTER SYSTEM TO MODEL 152 AND 150 LASER SYSTEM?

BLUE GREEN FILTER SYSTEM TO MODEL 152 AND 150 LASER SYSTEM is a medical device that received FDA 510(k) clearance on 1983-03-22. The listed applicant is Britt Corp., Inc.. The 510(k) number is K837151.

When did BLUE GREEN FILTER SYSTEM TO MODEL 152 AND 150 LASER SYSTEM receive FDA 510(k) clearance?

BLUE GREEN FILTER SYSTEM TO MODEL 152 AND 150 LASER SYSTEM received FDA 510(k) clearance on 1983-03-22, under 510(k) number K837151.

Who is the listed applicant for BLUE GREEN FILTER SYSTEM TO MODEL 152 AND 150 LASER SYSTEM?

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

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Other records listing Britt Corp., Inc. as applicant

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.

K003828VASO PRESS DVT FOOT GARMENT #VP 520K991038VASO PRESS DVT SYSTEM, MODELS VP500, VP501K974393VASO PRESS SYSTEMK860977MODEL 545-45 FOR NEUROLOGICAL SURGICAL APPLICATIONK860975MODEL 545-45 LASER FOR EAR, NOSE & THROATK860974MODEL 545-45 LASER FOR DERMA., POD., SURGICAL

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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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