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FDA 510(k)

STERILE PISTON SYRINGE

K-Number: K002717 · 2001-01-08

ApplicantAbbott Laboratories
Decision Date2001-01-08
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERILE PISTON SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Abbott Laboratories. It received FDA 510(k) clearance on 2001-01-08 under 510(k) number K002717. 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 PISTON SYRINGE?

STERILE PISTON SYRINGE is a medical device that received FDA 510(k) clearance on 2001-01-08. The listed applicant is Abbott Laboratories. The 510(k) number is K002717.

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

STERILE PISTON SYRINGE received FDA 510(k) clearance on 2001-01-08, under 510(k) number K002717.

Who is the listed applicant for STERILE PISTON SYRINGE?

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

What is the FDA product code for STERILE PISTON SYRINGE?

The FDA product code for STERILE PISTON 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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