FRESH CELLS NCI H292
K-Number: K973210 · 1997-09-25
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Device Summary
Frequently Asked Questions
What is the FRESH CELLS NCI H292?
FRESH CELLS NCI H292 is a medical device that received FDA 510(k) clearance on 1997-09-25. The listed applicant is Diagnostic Hybrids, Inc.. The 510(k) number is K973210.
When did FRESH CELLS NCI H292 receive FDA 510(k) clearance?
FRESH CELLS NCI H292 received FDA 510(k) clearance on 1997-09-25, under 510(k) number K973210.
Who is the listed applicant for FRESH CELLS NCI H292?
The FDA 510(k) record lists Diagnostic Hybrids, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for FRESH CELLS NCI H292?
The FDA product code for FRESH CELLS NCI H292 is KIR.
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 Diagnostic Hybrids, 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: KIR)
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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