INOX THERMOMETER JAR
K-Number: K852301 · 1985-07-01
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Device Summary
Frequently Asked Questions
What is the INOX THERMOMETER JAR?
INOX THERMOMETER JAR is a medical device that received FDA 510(k) clearance on 1985-07-01. The listed applicant is Broadwest Corp.. The 510(k) number is K852301.
When did INOX THERMOMETER JAR receive FDA 510(k) clearance?
INOX THERMOMETER JAR received FDA 510(k) clearance on 1985-07-01, under 510(k) number K852301.
Who is the listed applicant for INOX THERMOMETER JAR?
The FDA 510(k) record lists Broadwest Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INOX THERMOMETER JAR?
The FDA product code for INOX THERMOMETER JAR is FLK.
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 Broadwest 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: FLK)
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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