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FDA 510(k)

CHATTANOOGA DRY HEAT WHIRLPOOL, MODEL 2000

K-Number: K011243 · 2001-07-06

ApplicantChattanooga Group, Inc.
Decision Date2001-07-06
Product CodeLSB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CHATTANOOGA DRY HEAT WHIRLPOOL, MODEL 2000 is the device name listed in this FDA 510(k) record. The listed applicant is Chattanooga Group, Inc.. It received FDA 510(k) clearance on 2001-07-06 under 510(k) number K011243. The device is classified under product code LSB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHATTANOOGA DRY HEAT WHIRLPOOL, MODEL 2000?

CHATTANOOGA DRY HEAT WHIRLPOOL, MODEL 2000 is a medical device that received FDA 510(k) clearance on 2001-07-06. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K011243.

When did CHATTANOOGA DRY HEAT WHIRLPOOL, MODEL 2000 receive FDA 510(k) clearance?

CHATTANOOGA DRY HEAT WHIRLPOOL, MODEL 2000 received FDA 510(k) clearance on 2001-07-06, under 510(k) number K011243.

Who is the listed applicant for CHATTANOOGA DRY HEAT WHIRLPOOL, MODEL 2000?

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

What is the FDA product code for CHATTANOOGA DRY HEAT WHIRLPOOL, MODEL 2000?

The FDA product code for CHATTANOOGA DRY HEAT WHIRLPOOL, MODEL 2000 is LSB.

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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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