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FDA 510(k)

VECTRA PRO MODELS 2 AND 4

K-Number: K982324 · 1999-02-01

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

Device Summary

VECTRA PRO MODELS 2 AND 4 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 K982324. 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 PRO MODELS 2 AND 4?

VECTRA PRO MODELS 2 AND 4 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 K982324.

When did VECTRA PRO MODELS 2 AND 4 receive FDA 510(k) clearance?

VECTRA PRO MODELS 2 AND 4 received FDA 510(k) clearance on 1999-02-01, under 510(k) number K982324.

Who is the listed applicant for VECTRA PRO MODELS 2 AND 4?

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 PRO MODELS 2 AND 4?

The FDA product code for VECTRA PRO MODELS 2 AND 4 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.

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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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