PRO-FLEX, DIGITAL THERMOMETER WITH FLEXIBLE PROBE
K-Number: K961357 · 1996-08-16
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Device Summary
Frequently Asked Questions
What is the PRO-FLEX, DIGITAL THERMOMETER WITH FLEXIBLE PROBE?
PRO-FLEX, DIGITAL THERMOMETER WITH FLEXIBLE PROBE is a medical device that received FDA 510(k) clearance on 1996-08-16. The listed applicant is Intelligent Product Limited Co.. The 510(k) number is K961357.
When did PRO-FLEX, DIGITAL THERMOMETER WITH FLEXIBLE PROBE receive FDA 510(k) clearance?
PRO-FLEX, DIGITAL THERMOMETER WITH FLEXIBLE PROBE received FDA 510(k) clearance on 1996-08-16, under 510(k) number K961357.
Who is the listed applicant for PRO-FLEX, DIGITAL THERMOMETER WITH FLEXIBLE PROBE?
The FDA 510(k) record lists Intelligent Product Limited Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PRO-FLEX, DIGITAL THERMOMETER WITH FLEXIBLE PROBE?
The FDA product code for PRO-FLEX, DIGITAL THERMOMETER WITH FLEXIBLE PROBE 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 Intelligent Product Limited 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.
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