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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 the device name listed in this FDA 510(k) record. The listed applicant is 3nt Medical , Ltd.. It received FDA 510(k) clearance on 2021-07-23 under 510(k) 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. The listed applicant is 3nt Medical , Ltd.. The 510(k) number is K202727.

When did Peregrine Endoscopy System receive FDA 510(k) clearance?

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

Who is the listed applicant for Peregrine Endoscopy System?

The FDA 510(k) record lists 3nt Medical , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Peregrine Endoscopy System?

The FDA product code for Peregrine Endoscopy System is EOB.

Other records listing 3nt Medical , Ltd. 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.

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Related Devices (Code: EOB)

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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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