TIMETER PRODUCED SCHRADER OXYGEN ADAPTOR
K-Number: K811549 · 1981-06-18
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Device Summary
Frequently Asked Questions
What is the TIMETER PRODUCED SCHRADER OXYGEN ADAPTOR?
TIMETER PRODUCED SCHRADER 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 K811549.
When did TIMETER PRODUCED SCHRADER OXYGEN ADAPTOR receive FDA 510(k) clearance?
TIMETER PRODUCED SCHRADER OXYGEN ADAPTOR received FDA 510(k) clearance on 1981-06-18, under 510(k) number K811549.
Who is the listed applicant for TIMETER PRODUCED SCHRADER 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 SCHRADER OXYGEN ADAPTOR?
The FDA product code for TIMETER PRODUCED SCHRADER 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.
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
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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