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FDA 510(k)

PRINCESS SYRINGE

K-Number: K980577 · 1998-05-08

ApplicantSodexco
Decision Date1998-05-08
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PRINCESS SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Sodexco. It received FDA 510(k) clearance on 1998-05-08 under 510(k) number K980577. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRINCESS SYRINGE?

PRINCESS SYRINGE is a medical device that received FDA 510(k) clearance on 1998-05-08. The listed applicant is Sodexco. The 510(k) number is K980577.

When did PRINCESS SYRINGE receive FDA 510(k) clearance?

PRINCESS SYRINGE received FDA 510(k) clearance on 1998-05-08, under 510(k) number K980577.

Who is the listed applicant for PRINCESS SYRINGE?

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

What is the FDA product code for PRINCESS SYRINGE?

The FDA product code for PRINCESS SYRINGE is EIA.

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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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