PLATELET-CHEX FOR BLOOD CENTERS
K-Number: K792467 · 1979-12-31
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Device Summary
Frequently Asked Questions
What is the PLATELET-CHEX FOR BLOOD CENTERS?
PLATELET-CHEX FOR BLOOD CENTERS is a medical device that received FDA 510(k) clearance on 1979-12-31. The listed applicant is Streck Laboratories, Inc.. The 510(k) number is K792467.
When did PLATELET-CHEX FOR BLOOD CENTERS receive FDA 510(k) clearance?
PLATELET-CHEX FOR BLOOD CENTERS received FDA 510(k) clearance on 1979-12-31, under 510(k) number K792467.
Who is the listed applicant for PLATELET-CHEX FOR BLOOD CENTERS?
The FDA 510(k) record lists Streck Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PLATELET-CHEX FOR BLOOD CENTERS?
The FDA product code for PLATELET-CHEX FOR BLOOD CENTERS is JPK.
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 Streck Laboratories, 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: JPK)
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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