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FDA 510(k)

PISTON SYRINGE DISPOS. STERILE SYRING

K-Number: K840192 · 1984-03-06

ApplicantInterexpo Corp.
Decision Date1984-03-06
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PISTON SYRINGE DISPOS. STERILE SYRING is the device name listed in this FDA 510(k) record. The listed applicant is Interexpo Corp.. It received FDA 510(k) clearance on 1984-03-06 under 510(k) number K840192. 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 PISTON SYRINGE DISPOS. STERILE SYRING?

PISTON SYRINGE DISPOS. STERILE SYRING is a medical device that received FDA 510(k) clearance on 1984-03-06. The listed applicant is Interexpo Corp.. The 510(k) number is K840192.

When did PISTON SYRINGE DISPOS. STERILE SYRING receive FDA 510(k) clearance?

PISTON SYRINGE DISPOS. STERILE SYRING received FDA 510(k) clearance on 1984-03-06, under 510(k) number K840192.

Who is the listed applicant for PISTON SYRINGE DISPOS. STERILE SYRING?

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

What is the FDA product code for PISTON SYRINGE DISPOS. STERILE SYRING?

The FDA product code for PISTON SYRINGE DISPOS. STERILE SYRING is FMF.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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