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FDA 510(k)

STERILE AIR SYRINGE

K-Number: K780550 · 1978-04-19

ApplicantNational Patent Development Corp.
Decision Date1978-04-19
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERILE AIR SYRINGE 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 1978-04-19 under 510(k) number K780550. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STERILE AIR SYRINGE?

STERILE AIR SYRINGE is a medical device that received FDA 510(k) clearance on 1978-04-19. The listed applicant is National Patent Development Corp.. The 510(k) number is K780550.

When did STERILE AIR SYRINGE receive FDA 510(k) clearance?

STERILE AIR SYRINGE received FDA 510(k) clearance on 1978-04-19, under 510(k) number K780550.

Who is the listed applicant for STERILE AIR SYRINGE?

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 STERILE AIR SYRINGE?

The FDA product code for STERILE AIR SYRINGE is FMF.

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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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