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FDA 510(k)

VECTRA STIM MODELS 200 AND 400

K-Number: K982321 · 1999-02-01

ApplicantChattanooga Group, Inc.
Decision Date1999-02-01
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

VECTRA STIM MODELS 200 AND 400 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 1999-02-01 under 510(k) number K982321. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VECTRA STIM MODELS 200 AND 400?

VECTRA STIM MODELS 200 AND 400 is a medical device that received FDA 510(k) clearance on 1999-02-01. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K982321.

When did VECTRA STIM MODELS 200 AND 400 receive FDA 510(k) clearance?

VECTRA STIM MODELS 200 AND 400 received FDA 510(k) clearance on 1999-02-01, under 510(k) number K982321.

Who is the listed applicant for VECTRA STIM MODELS 200 AND 400?

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 VECTRA STIM MODELS 200 AND 400?

The FDA product code for VECTRA STIM MODELS 200 AND 400 is GZJ.

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Other records listing Chattanooga Group, Inc. 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.

K011243CHATTANOOGA DRY HEAT WHIRLPOOL, MODEL 2000K982317VECTRA COMBOK982324VECTRA PRO MODELS 2 AND 4K982828FORTE, MODELS CPS 400 STIM, CPS 200 STIMK982829FORTE, MODEL CPS ULTRASOUNDK982830FORTE, MODELS CPS 400 COMBO, CPS 200 COMBO

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Related Devices (Code: GZJ)

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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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