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FDA 510(k)

PANORET, MODEL 1000A

K-Number: K001111 · 2000-07-07

ApplicantCmt Medical Technologies, Ltd.
Decision Date2000-07-07
Product CodeHKL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PANORET, MODEL 1000A is the device name listed in this FDA 510(k) record. The listed applicant is Cmt Medical Technologies, Ltd.. It received FDA 510(k) clearance on 2000-07-07 under 510(k) number K001111. The device is classified under product code HKL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PANORET, MODEL 1000A?

PANORET, MODEL 1000A is a medical device that received FDA 510(k) clearance on 2000-07-07. The listed applicant is Cmt Medical Technologies, Ltd.. The 510(k) number is K001111.

When did PANORET, MODEL 1000A receive FDA 510(k) clearance?

PANORET, MODEL 1000A received FDA 510(k) clearance on 2000-07-07, under 510(k) number K001111.

Who is the listed applicant for PANORET, MODEL 1000A?

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

What is the FDA product code for PANORET, MODEL 1000A?

The FDA product code for PANORET, MODEL 1000A is HKL.

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Other records listing Cmt Medical Technologies, Ltd. as applicant

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Related Devices (Code: HKL)

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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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