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FDA 510(k)

NEEDLE II, BURRON FILTER

K-Number: K790060 · 1979-03-21

ApplicantNational Patent Development Corp.
Decision Date1979-03-21
Product CodeGAA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NEEDLE II, BURRON FILTER is the device name listed in this FDA 510(k) record. The listed applicant is National Patent Development Corp.. It received FDA 510(k) clearance on 1979-03-21 under 510(k) number K790060. The device is classified under product code GAA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEEDLE II, BURRON FILTER?

NEEDLE II, BURRON FILTER is a medical device that received FDA 510(k) clearance on 1979-03-21. The listed applicant is National Patent Development Corp.. The 510(k) number is K790060.

When did NEEDLE II, BURRON FILTER receive FDA 510(k) clearance?

NEEDLE II, BURRON FILTER received FDA 510(k) clearance on 1979-03-21, under 510(k) number K790060.

Who is the listed applicant for NEEDLE II, BURRON FILTER?

The FDA 510(k) record lists National Patent Development Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEEDLE II, BURRON FILTER?

The FDA product code for NEEDLE II, BURRON FILTER is GAA.

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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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