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FDA 510(k)

VECTRA (INTELECT) EPR ULTRASOUND

K-Number: K031116 · 2003-12-03

ApplicantChattanooga Group
Decision Date2003-12-03
Product CodeIMI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

VECTRA (INTELECT) EPR ULTRASOUND is the device name listed in this FDA 510(k) record. The listed applicant is Chattanooga Group. It received FDA 510(k) clearance on 2003-12-03 under 510(k) number K031116. The device is classified under product code IMI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VECTRA (INTELECT) EPR ULTRASOUND?

VECTRA (INTELECT) EPR ULTRASOUND is a medical device that received FDA 510(k) clearance on 2003-12-03. The listed applicant is Chattanooga Group. The 510(k) number is K031116.

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

VECTRA (INTELECT) EPR ULTRASOUND received FDA 510(k) clearance on 2003-12-03, under 510(k) number K031116.

Who is the listed applicant for VECTRA (INTELECT) EPR ULTRASOUND?

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 (INTELECT) EPR ULTRASOUND?

The FDA product code for VECTRA (INTELECT) EPR ULTRASOUND is IMI.

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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: IMI)

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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