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FDA 510(k)

VECTRA EPR SYSTEM AND INTELECT EPR SYSTEM

K-Number: K031077 · 2003-12-11

ApplicantChattanooga Group
Decision Date2003-12-11
Product CodeIMG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

VECTRA EPR SYSTEM AND INTELECT EPR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Chattanooga Group. It received FDA 510(k) clearance on 2003-12-11 under 510(k) number K031077. The device is classified under product code IMG. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VECTRA EPR SYSTEM AND INTELECT EPR SYSTEM?

VECTRA EPR SYSTEM AND INTELECT EPR SYSTEM is a medical device that received FDA 510(k) clearance on 2003-12-11. The listed applicant is Chattanooga Group. The 510(k) number is K031077.

When did VECTRA EPR SYSTEM AND INTELECT EPR SYSTEM receive FDA 510(k) clearance?

VECTRA EPR SYSTEM AND INTELECT EPR SYSTEM received FDA 510(k) clearance on 2003-12-11, under 510(k) number K031077.

Who is the listed applicant for VECTRA EPR SYSTEM AND INTELECT EPR SYSTEM?

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

What is the FDA product code for VECTRA EPR SYSTEM AND INTELECT EPR SYSTEM?

The FDA product code for VECTRA EPR SYSTEM AND INTELECT EPR SYSTEM is IMG.

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Other records listing Chattanooga Group 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.

K090632COMPEX REHABK083433INTELECT SWD 100, MODEL 1600; SENIOR SOLUTIONS SHORTWAVE DIATHERMY, MODEL 1601K083140COMPEX SPORT PLUSK070425VITALSTIM EXPERIAK053223TRITON/TRU-TRAC/TX/TRITON DTS TRACTIONK051938TRITON/TRU-TRAC/TX TRACTION DEVICES

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Related Devices (Code: IMG)

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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