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FDA 510(k)

REGULATOR, OXYGEN MECHANICAL

K-Number: K803207 · 1981-01-15

ApplicantTimeter Instrument Corp.
Decision Date1981-01-15
Product CodeCAN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

REGULATOR, OXYGEN MECHANICAL is the device name listed in this FDA 510(k) record. The listed applicant is Timeter Instrument Corp.. It received FDA 510(k) clearance on 1981-01-15 under 510(k) number K803207. 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 REGULATOR, OXYGEN MECHANICAL?

REGULATOR, OXYGEN MECHANICAL is a medical device that received FDA 510(k) clearance on 1981-01-15. The listed applicant is Timeter Instrument Corp.. The 510(k) number is K803207.

When did REGULATOR, OXYGEN MECHANICAL receive FDA 510(k) clearance?

REGULATOR, OXYGEN MECHANICAL received FDA 510(k) clearance on 1981-01-15, under 510(k) number K803207.

Who is the listed applicant for REGULATOR, OXYGEN MECHANICAL?

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

What is the FDA product code for REGULATOR, OXYGEN MECHANICAL?

The FDA product code for REGULATOR, OXYGEN MECHANICAL is CAN.

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Other records listing Timeter Instrument Corp. 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.

K875075RT-200 COMPUTER INTERFACEK875074VACUMATE INTERMITTENT/CONTINUOUS CONTROLLER,VM2000K871603CRITERION II & IIA OXYGEN CONCENTRATORSK864836L.A.P. SPIROMETERK834274CRITERION IK823775BORDON GAGE REGULATOR #BG

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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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