RETRIEVAL BAG
K-Number: K123728 · 2013-12-11
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Device Summary
Frequently Asked Questions
What is the RETRIEVAL BAG?
RETRIEVAL BAG is a medical device that received FDA 510(k) clearance on 2013-12-11. The listed applicant is Flexbar Machine Corp.. The 510(k) number is K123728.
When did RETRIEVAL BAG receive FDA 510(k) clearance?
RETRIEVAL BAG received FDA 510(k) clearance on 2013-12-11, under 510(k) number K123728.
Who is the listed applicant for RETRIEVAL BAG?
The FDA 510(k) record lists Flexbar Machine Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for RETRIEVAL BAG?
The FDA product code for 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 Flexbar Machine 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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