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FDA 510(k)

UNIVEC BIFURCATED SLIDING SHEATH SYRINGE

K-Number: K020500 · 2002-03-19

ApplicantUnivec, Inc.
Decision Date2002-03-19
Product CodeSCL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

UNIVEC BIFURCATED SLIDING SHEATH SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Univec, Inc.. It received FDA 510(k) clearance on 2002-03-19 under 510(k) number K020500. The device is classified under product code SCL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UNIVEC BIFURCATED SLIDING SHEATH SYRINGE?

UNIVEC BIFURCATED SLIDING SHEATH SYRINGE is a medical device that received FDA 510(k) clearance on 2002-03-19. The listed applicant is Univec, Inc.. The 510(k) number is K020500.

When did UNIVEC BIFURCATED SLIDING SHEATH SYRINGE receive FDA 510(k) clearance?

UNIVEC BIFURCATED SLIDING SHEATH SYRINGE received FDA 510(k) clearance on 2002-03-19, under 510(k) number K020500.

Who is the listed applicant for UNIVEC BIFURCATED SLIDING SHEATH SYRINGE?

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

What is the FDA product code for UNIVEC BIFURCATED SLIDING SHEATH SYRINGE?

The FDA product code for UNIVEC BIFURCATED SLIDING SHEATH SYRINGE is SCL.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Univec, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: SCL)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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