MODEL 143 SERIES BLOOD PRODUCT IRRADIATORS
K-Number: K915767 · 1995-07-12
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Device Summary
Frequently Asked Questions
What is the MODEL 143 SERIES BLOOD PRODUCT IRRADIATORS?
MODEL 143 SERIES BLOOD PRODUCT IRRADIATORS is a medical device that received FDA 510(k) clearance on 1995-07-12. The listed applicant is J. L. Shepherd and Assoc.. The 510(k) number is K915767.
When did MODEL 143 SERIES BLOOD PRODUCT IRRADIATORS receive FDA 510(k) clearance?
MODEL 143 SERIES BLOOD PRODUCT IRRADIATORS received FDA 510(k) clearance on 1995-07-12, under 510(k) number K915767.
Who is the listed applicant for MODEL 143 SERIES BLOOD PRODUCT IRRADIATORS?
The FDA 510(k) record lists J. L. Shepherd and Assoc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODEL 143 SERIES BLOOD PRODUCT IRRADIATORS?
The FDA product code for MODEL 143 SERIES BLOOD PRODUCT IRRADIATORS is MOT.
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 J. L. Shepherd and Assoc. 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: MOT)
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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