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FDA 510(k)

TIMETER PRODUCED OHIO OXYGEN ADAPTOR

K-Number: K811551 · 1981-06-18

Decision Date1981-06-18
Product CodeBYX
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TIMETER PRODUCED OHIO OXYGEN ADAPTOR 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 1981-06-18 under 510(k) number K811551. The device is classified under product code BYX. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TIMETER PRODUCED OHIO OXYGEN ADAPTOR?

TIMETER PRODUCED OHIO OXYGEN ADAPTOR is a medical device that received FDA 510(k) clearance on 1981-06-18. The listed applicant is Timeter Instrument Corp.. The 510(k) number is K811551.

When did TIMETER PRODUCED OHIO OXYGEN ADAPTOR receive FDA 510(k) clearance?

TIMETER PRODUCED OHIO OXYGEN ADAPTOR received FDA 510(k) clearance on 1981-06-18, under 510(k) number K811551.

Who is the listed applicant for TIMETER PRODUCED OHIO OXYGEN ADAPTOR?

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 TIMETER PRODUCED OHIO OXYGEN ADAPTOR?

The FDA product code for TIMETER PRODUCED OHIO OXYGEN ADAPTOR is BYX.

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.

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.

View all 29 devices →

Related Devices (Code: BYX)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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