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FDA 510(k)

IFA ANTI-NDNA

K-Number: K771376 · 1977-10-18

ApplicantElectro-Nucleonics Laboratories, Inc.
Decision Date1977-10-18
Product CodeDHN
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

IFA ANTI-NDNA is the device name listed in this FDA 510(k) record. The listed applicant is Electro-Nucleonics Laboratories, Inc.. It received FDA 510(k) clearance on 1977-10-18 under 510(k) number K771376. The device is classified under product code DHN. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IFA ANTI-NDNA?

IFA ANTI-NDNA is a medical device that received FDA 510(k) clearance on 1977-10-18. The listed applicant is Electro-Nucleonics Laboratories, Inc.. The 510(k) number is K771376.

When did IFA ANTI-NDNA receive FDA 510(k) clearance?

IFA ANTI-NDNA received FDA 510(k) clearance on 1977-10-18, under 510(k) number K771376.

Who is the listed applicant for IFA ANTI-NDNA?

The FDA 510(k) record lists Electro-Nucleonics Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IFA ANTI-NDNA?

The FDA product code for IFA ANTI-NDNA is DHN.

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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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