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FDA 510(k)

FROLOV'S RESPIRATION TRAINING DEVICE, FRTD-01

K-Number: K992256 · 2000-01-11

ApplicantIntercontinental New Technologies, Inc.
Decision Date2000-01-11
Product CodeBWF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

FROLOV'S RESPIRATION TRAINING DEVICE, FRTD-01 is the device name listed in this FDA 510(k) record. The listed applicant is Intercontinental New Technologies, Inc.. It received FDA 510(k) clearance on 2000-01-11 under 510(k) number K992256. The device is classified under product code BWF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FROLOV'S RESPIRATION TRAINING DEVICE, FRTD-01?

FROLOV'S RESPIRATION TRAINING DEVICE, FRTD-01 is a medical device that received FDA 510(k) clearance on 2000-01-11. The listed applicant is Intercontinental New Technologies, Inc.. The 510(k) number is K992256.

When did FROLOV'S RESPIRATION TRAINING DEVICE, FRTD-01 receive FDA 510(k) clearance?

FROLOV'S RESPIRATION TRAINING DEVICE, FRTD-01 received FDA 510(k) clearance on 2000-01-11, under 510(k) number K992256.

Who is the listed applicant for FROLOV'S RESPIRATION TRAINING DEVICE, FRTD-01?

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

What is the FDA product code for FROLOV'S RESPIRATION TRAINING DEVICE, FRTD-01?

The FDA product code for FROLOV'S RESPIRATION TRAINING DEVICE, FRTD-01 is BWF.

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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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