TEMPERATURE MONITOR
K-Number: K772217 · 1977-12-13
Advertisement
Device Summary
Frequently Asked Questions
What is the TEMPERATURE MONITOR?
TEMPERATURE MONITOR is a medical device that received FDA 510(k) clearance on 1977-12-13. The listed applicant is Hudson Oxygen Therapy Sales Co.. The 510(k) number is K772217.
When did TEMPERATURE MONITOR receive FDA 510(k) clearance?
TEMPERATURE MONITOR received FDA 510(k) clearance on 1977-12-13, under 510(k) number K772217.
Who is the listed applicant for TEMPERATURE MONITOR?
The FDA 510(k) record lists Hudson Oxygen Therapy Sales Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TEMPERATURE MONITOR?
The FDA product code for TEMPERATURE MONITOR is FLL.
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 Hudson Oxygen Therapy Sales Co. 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: FLL)
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.
Advertisement