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FDA 510(k)

Peregrine Endoscopy System

K-Number: K202727 · 2021-07-23

Applicant3nt Medical , Ltd.
Decision Date2021-07-23
Product CodeEOB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

Peregrine Endoscopy System is a medical device manufactured by 3nt Medical , Ltd.. It received FDA 510(k) clearance on 2021-07-23 under approval number K202727. The device is classified under product code EOB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Peregrine Endoscopy System?

Peregrine Endoscopy System is a medical device that received FDA 510(k) clearance on 2021-07-23. It is manufactured by 3nt Medical , Ltd.. The 510(k) number is K202727.

When was Peregrine Endoscopy System approved by the FDA?

Peregrine Endoscopy System received FDA 510(k) clearance on 2021-07-23, under approval number K202727.

What company makes Peregrine Endoscopy System?

Peregrine Endoscopy System is manufactured by 3nt Medical , Ltd..

What is the FDA product code for Peregrine Endoscopy System?

The FDA product code for Peregrine Endoscopy System is EOB.

Related Clinical Trials

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Other Devices by 3nt Medical , Ltd.

K1629163NT endoscopy system K181838Sinusway Dilation System K192305Colibri Endoscopy System

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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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