FDA 510(k)

DANTEC ELECTRODES MODEL DNE 116, 117 & 13P02/12

K-Number: K896874 · 1990-06-18

Decision Date1990-06-18

Product CodeIKT

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

DANTEC ELECTRODES MODEL DNE 116, 117 & 13P02/12 is the device name listed in this FDA 510(k) record. The listed applicant is Dantec Medical, Inc.. It received FDA 510(k) clearance on 1990-06-18 under 510(k) number K896874. The device is classified under product code IKT. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DANTEC ELECTRODES MODEL DNE 116, 117 & 13P02/12?

DANTEC ELECTRODES MODEL DNE 116, 117 & 13P02/12 is a medical device that received FDA 510(k) clearance on 1990-06-18. The listed applicant is Dantec Medical, Inc.. The 510(k) number is K896874.

When did DANTEC ELECTRODES MODEL DNE 116, 117 & 13P02/12 receive FDA 510(k) clearance?

DANTEC ELECTRODES MODEL DNE 116, 117 & 13P02/12 received FDA 510(k) clearance on 1990-06-18, under 510(k) number K896874.

Who is the listed applicant for DANTEC ELECTRODES MODEL DNE 116, 117 & 13P02/12?

The FDA 510(k) record lists Dantec Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DANTEC ELECTRODES MODEL DNE 116, 117 & 13P02/12?

The FDA product code for DANTEC ELECTRODES MODEL DNE 116, 117 & 13P02/12 is IKT.

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Other records listing Dantec Medical, Inc. as applicant

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Related Devices (Code: IKT)

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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.