BODILY FLUID DISPOSAL KIT
K-Number: K944880 · 1994-12-15
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Device Summary
Frequently Asked Questions
What is the BODILY FLUID DISPOSAL KIT?
BODILY FLUID DISPOSAL KIT is a medical device that received FDA 510(k) clearance on 1994-12-15. The listed applicant is Clinical Resources, Inc.. The 510(k) number is K944880.
When did BODILY FLUID DISPOSAL KIT receive FDA 510(k) clearance?
BODILY FLUID DISPOSAL KIT received FDA 510(k) clearance on 1994-12-15, under 510(k) number K944880.
Who is the listed applicant for BODILY FLUID DISPOSAL KIT?
The FDA 510(k) record lists Clinical Resources, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BODILY FLUID DISPOSAL KIT?
The FDA product code for BODILY FLUID DISPOSAL KIT is FXX.
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 Clinical Resources, 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: FXX)
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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