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FDA 510(k)

0.9% SODIUM CHLORIDE DILUENT IN PLASTIC SYRINGE

K-Number: K953805 · 1996-06-28

ApplicantAbbott Laboratories
Decision Date1996-06-28
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

0.9% SODIUM CHLORIDE DILUENT IN PLASTIC 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 1996-06-28 under 510(k) number K953805. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 0.9% SODIUM CHLORIDE DILUENT IN PLASTIC SYRINGE?

0.9% SODIUM CHLORIDE DILUENT IN PLASTIC SYRINGE is a medical device that received FDA 510(k) clearance on 1996-06-28. The listed applicant is Abbott Laboratories. The 510(k) number is K953805.

When did 0.9% SODIUM CHLORIDE DILUENT IN PLASTIC SYRINGE receive FDA 510(k) clearance?

0.9% SODIUM CHLORIDE DILUENT IN PLASTIC SYRINGE received FDA 510(k) clearance on 1996-06-28, under 510(k) number K953805.

Who is the listed applicant for 0.9% SODIUM CHLORIDE DILUENT IN PLASTIC 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 0.9% SODIUM CHLORIDE DILUENT IN PLASTIC SYRINGE?

The FDA product code for 0.9% SODIUM CHLORIDE DILUENT IN PLASTIC SYRINGE is FOZ.

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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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