URESIL SPECIMEN RETRIEVAL BAG
K-Number: K923219 · 1992-12-15
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Device Summary
Frequently Asked Questions
What is the URESIL SPECIMEN RETRIEVAL BAG?
URESIL SPECIMEN RETRIEVAL BAG is a medical device that received FDA 510(k) clearance on 1992-12-15. The listed applicant is Uresil Corp.. The 510(k) number is K923219.
When did URESIL SPECIMEN RETRIEVAL BAG receive FDA 510(k) clearance?
URESIL SPECIMEN RETRIEVAL BAG received FDA 510(k) clearance on 1992-12-15, under 510(k) number K923219.
Who is the listed applicant for URESIL SPECIMEN RETRIEVAL BAG?
The FDA 510(k) record lists Uresil Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for URESIL SPECIMEN RETRIEVAL BAG?
The FDA product code for URESIL SPECIMEN RETRIEVAL BAG is GCJ.
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 Uresil Corp. 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: GCJ)
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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