BLOOD CONTAINMENT PACK
K-Number: K872448 · 1987-11-17
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Device Summary
Frequently Asked Questions
What is the BLOOD CONTAINMENT PACK?
BLOOD CONTAINMENT PACK is a medical device that received FDA 510(k) clearance on 1987-11-17. The listed applicant is Professional Medical Services. The 510(k) number is K872448.
When did BLOOD CONTAINMENT PACK receive FDA 510(k) clearance?
BLOOD CONTAINMENT PACK received FDA 510(k) clearance on 1987-11-17, under 510(k) number K872448.
Who is the listed applicant for BLOOD CONTAINMENT PACK?
The FDA 510(k) record lists Professional Medical Services as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BLOOD CONTAINMENT PACK?
The FDA product code for BLOOD CONTAINMENT PACK is LRO.
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 Professional Medical Services 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: LRO)
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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