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MiniCap III CO2 Detector

by Minesafety Appliances Co.

510(k) K903200

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK903200 Date21 Sep 1990ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
CCK
Device Class
Class II
Regulation
21 CFR Part 868.1400
Advisory Committee
Anesthesiology
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 24 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

The MiniCap III CO2 Detector is a carbon-dioxide gas analyzer for gaseous-phase medical use in the gaseous phase. It is classified under product code CCK and is intended for use in anesthesiology.

The device received FDA 510(k) clearance under number K903200 on September 21, 1990, and was found substantially equivalent to a predicate device. It is manufactured by Minesafety Appliances Co. and is regulated as a medical device under the anesthesiology specialty.

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