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FDA 510(k)

CRT PORTABLE EMERGENCY OXYGEN INHALATOR

K-Number: K872170 · 1987-09-03

ApplicantCost Reduction Technologies, Inc.
Decision Date1987-09-03
Product CodeCAN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CRT PORTABLE EMERGENCY OXYGEN INHALATOR is the device name listed in this FDA 510(k) record. The listed applicant is Cost Reduction Technologies, Inc.. It received FDA 510(k) clearance on 1987-09-03 under 510(k) number K872170. The device is classified under product code CAN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CRT PORTABLE EMERGENCY OXYGEN INHALATOR?

CRT PORTABLE EMERGENCY OXYGEN INHALATOR is a medical device that received FDA 510(k) clearance on 1987-09-03. The listed applicant is Cost Reduction Technologies, Inc.. The 510(k) number is K872170.

When did CRT PORTABLE EMERGENCY OXYGEN INHALATOR receive FDA 510(k) clearance?

CRT PORTABLE EMERGENCY OXYGEN INHALATOR received FDA 510(k) clearance on 1987-09-03, under 510(k) number K872170.

Who is the listed applicant for CRT PORTABLE EMERGENCY OXYGEN INHALATOR?

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

What is the FDA product code for CRT PORTABLE EMERGENCY OXYGEN INHALATOR?

The FDA product code for CRT PORTABLE EMERGENCY OXYGEN INHALATOR is CAN.

Related Clinical Trials

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Related Devices (Code: CAN)

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.

K162811MR Conditional CGA 870Essex Industries, Inc.K080243PORTABLE OXYGEN UNIT SCA900San Cheong Co. , Ltd.K060265REMCORE REMOTE CONTROLLED OXYGEN REGULATORRemcore, Inc.K061785CYL-FIL OXYGEN SYSTEMResponsive Respiratory, Inc.K950777OXYGEN REGULATORMada Medical Products, Inc.K942751VANGUARD SERIES GAS REGULATORSBuckman Co., Inc.

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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