OXYGEN TWMER, MODEL SST
K-Number: K770424 · 1977-03-16
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Device Summary
Frequently Asked Questions
What is the OXYGEN TWMER, MODEL SST?
OXYGEN TWMER, MODEL SST is a medical device that received FDA 510(k) clearance on 1977-03-16. The listed applicant is Timeter Instrument Corp.. The 510(k) number is K770424.
When did OXYGEN TWMER, MODEL SST receive FDA 510(k) clearance?
OXYGEN TWMER, MODEL SST received FDA 510(k) clearance on 1977-03-16, under 510(k) number K770424.
Who is the listed applicant for OXYGEN TWMER, MODEL SST?
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 OXYGEN TWMER, MODEL SST?
The FDA product code for OXYGEN TWMER, MODEL SST is BXP.
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: BXP)
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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