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FDA 510(k)

MEDSCOPE

K-Number: K001314 · 2000-07-25

ApplicantAll-Pro Imaging Corp.
Decision Date2000-07-25
Product CodeHEX
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MEDSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is All-Pro Imaging Corp.. It received FDA 510(k) clearance on 2000-07-25 under 510(k) number K001314. The device is classified under product code HEX. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDSCOPE?

MEDSCOPE is a medical device that received FDA 510(k) clearance on 2000-07-25. The listed applicant is All-Pro Imaging Corp.. The 510(k) number is K001314.

When did MEDSCOPE receive FDA 510(k) clearance?

MEDSCOPE received FDA 510(k) clearance on 2000-07-25, under 510(k) number K001314.

Who is the listed applicant for MEDSCOPE?

The FDA 510(k) record lists All-Pro Imaging Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MEDSCOPE?

The FDA product code for MEDSCOPE is HEX.

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Other records listing All-Pro Imaging Corp. 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.

K001321ALL-PRO 2010K991435AII-PRO 100 PLUS AND ALL-PRO 200K911291ALL-PRO 100

Related Devices (Code: HEX)

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.

K233043Smart Scope® CXPeriwinkle Technologies Pvt., Ltd.K190187Gynescope SystemIllumigyn , Ltd.K182764Biop Digital ColposcopeBiop Medical , Ltd.K181034Pocket Colposcope SystemHadleigh Health Technologies, LLCK170446LT-300 SD Digital Video ColposcopeLutech Industries, Inc.K161871EVA (Enhanced Visual Assessment) SystemMobileodt , Ltd.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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