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FDA 510(k)

NEEDLES, STERILE, AIRWAY

K-Number: K770425 · 1977-04-15

ApplicantPfizer Pharmaceuticals
Decision Date1977-04-15
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NEEDLES, STERILE, AIRWAY is the device name listed in this FDA 510(k) record. The listed applicant is Pfizer Pharmaceuticals. It received FDA 510(k) clearance on 1977-04-15 under 510(k) number K770425. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEEDLES, STERILE, AIRWAY?

NEEDLES, STERILE, AIRWAY is a medical device that received FDA 510(k) clearance on 1977-04-15. The listed applicant is Pfizer Pharmaceuticals. The 510(k) number is K770425.

When did NEEDLES, STERILE, AIRWAY receive FDA 510(k) clearance?

NEEDLES, STERILE, AIRWAY received FDA 510(k) clearance on 1977-04-15, under 510(k) number K770425.

Who is the listed applicant for NEEDLES, STERILE, AIRWAY?

The FDA 510(k) record lists Pfizer Pharmaceuticals as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEEDLES, STERILE, AIRWAY?

The FDA product code for NEEDLES, STERILE, AIRWAY is FMI.

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Official Source

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