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FDA 510(k)

Disposable Specimen Retrieval Bag

K-Number: K201243 · 2020-07-10

ApplicantBeijing Biosis Healing Biolog Ical Technology Co., Ltd.
Decision Date2020-07-10
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

Disposable Specimen Retrieval Bag is a medical device manufactured by Beijing Biosis Healing Biolog Ical Technology Co., Ltd.. It received FDA 510(k) clearance on 2020-07-10 under approval number K201243. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Disposable Specimen Retrieval Bag?

Disposable Specimen Retrieval Bag is a medical device that received FDA 510(k) clearance on 2020-07-10. It is manufactured by Beijing Biosis Healing Biolog Ical Technology Co., Ltd.. The 510(k) number is K201243.

When was Disposable Specimen Retrieval Bag approved by the FDA?

Disposable Specimen Retrieval Bag received FDA 510(k) clearance on 2020-07-10, under approval number K201243.

What company makes Disposable Specimen Retrieval Bag?

Disposable Specimen Retrieval Bag is manufactured by Beijing Biosis Healing Biolog Ical Technology Co., Ltd..

What is the FDA product code for Disposable Specimen Retrieval Bag?

The FDA product code for Disposable Specimen Retrieval Bag is GCJ.

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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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