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FDA 510(k)

CAPOGEN Laser Cap

K-Number: K201854 · 2020-09-01

ApplicantNature, Inc.redible, Inc.
Decision Date2020-09-01
Product CodeOAP
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CAPOGEN Laser Cap is a medical device manufactured by Nature, Inc.redible, Inc.. It received FDA 510(k) clearance on 2020-09-01 under approval number K201854. The device is classified under product code OAP. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAPOGEN Laser Cap?

CAPOGEN Laser Cap is a medical device that received FDA 510(k) clearance on 2020-09-01. It is manufactured by Nature, Inc.redible, Inc.. The 510(k) number is K201854.

When was CAPOGEN Laser Cap approved by the FDA?

CAPOGEN Laser Cap received FDA 510(k) clearance on 2020-09-01, under approval number K201854.

What company makes CAPOGEN Laser Cap?

CAPOGEN Laser Cap is manufactured by Nature, Inc.redible, Inc..

What is the FDA product code for CAPOGEN Laser Cap?

The FDA product code for CAPOGEN Laser Cap is OAP.

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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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