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FDA 510(k)

NEEDLE, BURRON FILTER

K-Number: K790061 · 1979-02-16

ApplicantNational Patent Development Corp.
Decision Date1979-02-16
Product CodeGAA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

NEEDLE, 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 1979-02-16 under 510(k) number K790061. 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, BURRON FILTER?

NEEDLE, BURRON FILTER is a medical device that received FDA 510(k) clearance on 1979-02-16. The listed applicant is National Patent Development Corp.. The 510(k) number is K790061.

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

NEEDLE, BURRON FILTER received FDA 510(k) clearance on 1979-02-16, under 510(k) number K790061.

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

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

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Related Devices (Code: 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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