Specimen Retrieval Bag
K-Number: K172789 · 2018-02-01
Device Summary
Frequently Asked Questions
What is the Specimen Retrieval Bag?
Specimen Retrieval Bag is a medical device that received FDA 510(k) clearance on 2018-02-01. The listed applicant is Beijing Hangtian Kadi Technology R&D Institute. The 510(k) number is K172789.
When did Specimen Retrieval Bag receive FDA 510(k) clearance?
Specimen Retrieval Bag received FDA 510(k) clearance on 2018-02-01, under 510(k) number K172789.
Who is the listed applicant for Specimen Retrieval Bag?
The FDA 510(k) record lists Beijing Hangtian Kadi Technology R&D Institute as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Specimen Retrieval Bag?
The FDA product code for 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 Beijing Hangtian Kadi Technology R&D Institute 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.