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FDA 510(k)

INSIDE VIEW

K-Number: K001217 · 2000-07-11

ApplicantMonadnock Optics, Inc.
Decision Date2000-07-11
Product CodeGCM
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

INSIDE VIEW is the device name listed in this FDA 510(k) record. The listed applicant is Monadnock Optics, Inc.. It received FDA 510(k) clearance on 2000-07-11 under 510(k) number K001217. The device is classified under product code GCM. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSIDE VIEW?

INSIDE VIEW is a medical device that received FDA 510(k) clearance on 2000-07-11. The listed applicant is Monadnock Optics, Inc.. The 510(k) number is K001217.

When did INSIDE VIEW receive FDA 510(k) clearance?

INSIDE VIEW received FDA 510(k) clearance on 2000-07-11, under 510(k) number K001217.

Who is the listed applicant for INSIDE VIEW?

The FDA 510(k) record lists Monadnock Optics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INSIDE VIEW?

The FDA product code for INSIDE VIEW is GCM.

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Related Devices (Code: GCM)

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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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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