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FDA 510(k)

INTELECT 210 PORTABLE ULTRASOUND

K-Number: K841447 · 1984-05-09

ApplicantChattanooga Group, Inc.
Decision Date1984-05-09
Product CodeIMI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

INTELECT 210 PORTABLE ULTRASOUND 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 1984-05-09 under 510(k) number K841447. 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 INTELECT 210 PORTABLE ULTRASOUND?

INTELECT 210 PORTABLE ULTRASOUND is a medical device that received FDA 510(k) clearance on 1984-05-09. The listed applicant is Chattanooga Group, Inc.. The 510(k) number is K841447.

When did INTELECT 210 PORTABLE ULTRASOUND receive FDA 510(k) clearance?

INTELECT 210 PORTABLE ULTRASOUND received FDA 510(k) clearance on 1984-05-09, under 510(k) number K841447.

Who is the listed applicant for INTELECT 210 PORTABLE ULTRASOUND?

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 INTELECT 210 PORTABLE ULTRASOUND?

The FDA product code for INTELECT 210 PORTABLE ULTRASOUND is IMI.

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Other records listing Chattanooga Group, Inc. as applicant

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Related Devices (Code: IMI)

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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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