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FDA 510(k)

MODEL 525 - 25 WATT CO2 MEDICAL LASER/PODIATRY

K-Number: K860273 · 1986-04-23

ApplicantBritt Corp., Inc.
Decision Date1986-04-23
Product CodeGEX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MODEL 525 - 25 WATT CO2 MEDICAL LASER/PODIATRY 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 1986-04-23 under 510(k) number K860273. The device is classified under product code GEX. It was reviewed by the SU advisory panel. Product code GEX falls under the category of Gastroenterology, which includes gastrointestinal diagnostic and therapeutic devices. Devices in this category are subject to specific FDA regulatory requirements. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 525 - 25 WATT CO2 MEDICAL LASER/PODIATRY?

MODEL 525 - 25 WATT CO2 MEDICAL LASER/PODIATRY is a medical device that received FDA 510(k) clearance on 1986-04-23. The listed applicant is Britt Corp., Inc.. The 510(k) number is K860273.

When did MODEL 525 - 25 WATT CO2 MEDICAL LASER/PODIATRY receive FDA 510(k) clearance?

MODEL 525 - 25 WATT CO2 MEDICAL LASER/PODIATRY received FDA 510(k) clearance on 1986-04-23, under 510(k) number K860273.

Who is the listed applicant for MODEL 525 - 25 WATT CO2 MEDICAL LASER/PODIATRY?

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 MODEL 525 - 25 WATT CO2 MEDICAL LASER/PODIATRY?

The FDA product code for MODEL 525 - 25 WATT CO2 MEDICAL LASER/PODIATRY is GEX. This falls under the Gastroenterology category.

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Other records listing Britt Corp., Inc. as applicant

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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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