PLATELET CONTROL
K-Number: K780980 · 1978-07-27
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Device Summary
Frequently Asked Questions
What is the PLATELET CONTROL?
PLATELET CONTROL is a medical device that received FDA 510(k) clearance on 1978-07-27. The listed applicant is Bhp Diagnostix, Inc.. The 510(k) number is K780980.
When did PLATELET CONTROL receive FDA 510(k) clearance?
PLATELET CONTROL received FDA 510(k) clearance on 1978-07-27, under 510(k) number K780980.
Who is the listed applicant for PLATELET CONTROL?
The FDA 510(k) record lists Bhp Diagnostix, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PLATELET CONTROL?
The FDA product code for PLATELET CONTROL 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 Bhp Diagnostix, 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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