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FDA 510(k)

OXYGEN REGULATORS #50 PRT & BGT(BGT15,BGT18

K-Number: K852374 · 1985-07-12

ApplicantThe Timeter Group
Decision Date1985-07-12
Product CodeCAN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OXYGEN REGULATORS #50 PRT & BGT(BGT15,BGT18 is the device name listed in this FDA 510(k) record. The listed applicant is The Timeter Group. It received FDA 510(k) clearance on 1985-07-12 under 510(k) number K852374. 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 OXYGEN REGULATORS #50 PRT & BGT(BGT15,BGT18?

OXYGEN REGULATORS #50 PRT & BGT(BGT15,BGT18 is a medical device that received FDA 510(k) clearance on 1985-07-12. The listed applicant is The Timeter Group. The 510(k) number is K852374.

When did OXYGEN REGULATORS #50 PRT & BGT(BGT15,BGT18 receive FDA 510(k) clearance?

OXYGEN REGULATORS #50 PRT & BGT(BGT15,BGT18 received FDA 510(k) clearance on 1985-07-12, under 510(k) number K852374.

Who is the listed applicant for OXYGEN REGULATORS #50 PRT & BGT(BGT15,BGT18?

The FDA 510(k) record lists The Timeter Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OXYGEN REGULATORS #50 PRT & BGT(BGT15,BGT18?

The FDA product code for OXYGEN REGULATORS #50 PRT & BGT(BGT15,BGT18 is CAN.

Related Clinical Trials

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.

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Other records listing The Timeter Group 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.

K871452CLASSIC (TM) 200 OXYGEN FLOWMETERK862171MP-500 ELECTRONIC NEBULIZERK844556KHM 2000 DRIP WATCHER

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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