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FDA 510(k)

DELTA-NET

K-Number: K790341 · 1979-04-04

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1979-04-04
Product CodeKKX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DELTA-NET is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1979-04-04 under 510(k) number K790341. The device is classified under product code KKX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DELTA-NET?

DELTA-NET is a medical device that received FDA 510(k) clearance on 1979-04-04. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K790341.

When did DELTA-NET receive FDA 510(k) clearance?

DELTA-NET received FDA 510(k) clearance on 1979-04-04, under 510(k) number K790341.

Who is the listed applicant for DELTA-NET?

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

What is the FDA product code for DELTA-NET?

The FDA product code for DELTA-NET is KKX.

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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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