REDI-CHECK PHOTMETER Q.A.
K-Number: K923598 · 1992-10-14
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Device Summary
Frequently Asked Questions
What is the REDI-CHECK PHOTMETER Q.A.?
REDI-CHECK PHOTMETER Q.A. is a medical device that received FDA 510(k) clearance on 1992-10-14. The listed applicant is Awareness Technology, Inc.. The 510(k) number is K923598.
When did REDI-CHECK PHOTMETER Q.A. receive FDA 510(k) clearance?
REDI-CHECK PHOTMETER Q.A. received FDA 510(k) clearance on 1992-10-14, under 510(k) number K923598.
Who is the listed applicant for REDI-CHECK PHOTMETER Q.A.?
The FDA 510(k) record lists Awareness Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for REDI-CHECK PHOTMETER Q.A.?
The FDA product code for REDI-CHECK PHOTMETER Q.A. is JFS.
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 Awareness Technology, Inc. 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: JFS)
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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