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FDA 510(k)

STERILE FIELD SALINE AND HEPARIN LOCK FLUSH SYRINGES

K-Number: K053120 · 2005-12-09

ApplicantExcelsior Medical Corp.
Decision Date2005-12-09
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

STERILE FIELD SALINE AND HEPARIN LOCK FLUSH SYRINGES is the device name listed in this FDA 510(k) record. The listed applicant is Excelsior Medical Corp.. It received FDA 510(k) clearance on 2005-12-09 under 510(k) number K053120. 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 STERILE FIELD SALINE AND HEPARIN LOCK FLUSH SYRINGES?

STERILE FIELD SALINE AND HEPARIN LOCK FLUSH SYRINGES is a medical device that received FDA 510(k) clearance on 2005-12-09. The listed applicant is Excelsior Medical Corp.. The 510(k) number is K053120.

When did STERILE FIELD SALINE AND HEPARIN LOCK FLUSH SYRINGES receive FDA 510(k) clearance?

STERILE FIELD SALINE AND HEPARIN LOCK FLUSH SYRINGES received FDA 510(k) clearance on 2005-12-09, under 510(k) number K053120.

Who is the listed applicant for STERILE FIELD SALINE AND HEPARIN LOCK FLUSH SYRINGES?

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

What is the FDA product code for STERILE FIELD SALINE AND HEPARIN LOCK FLUSH SYRINGES?

The FDA product code for STERILE FIELD SALINE AND HEPARIN LOCK FLUSH SYRINGES is FOZ.

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Other records listing Excelsior Medical Corp. 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.

K130975SWABCAP AND SWABFLUSHK101270SWABFLSUH (3ML, 5ML, 10ML) MODEL 10331, 10351, 10311K083508SWABCAPK082837STERILE FIELD SALINE PRE-FILLED SYRINGE(S)K061497SYREX HEPARIN LOCK FLUSH SYRINGE, 1 UNIT/ML & 2 UNITS/MLK023740SYREX PRE-FILLED SYRINGE

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Related Devices (Code: FOZ)

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.

K260432Ruby Intravascular CatheterVenocare, Inc.K260165Unimpregnated Central Venous CatheterSpectrum VascularK261041ClearSafe Closed SystemMedSource Labs, LLCK260539MedSource QuickSafe™ Safety IV Catheter; MedSource PurSafe™ Safety IV CatheterMedSource Labs, LLCK253235Introcan Safety® Deep Access XL IV CatheterB.Braun Medical, Inc.K252137BD Insyte™ IV CatheterBecton Dickinson Infusion Therapy Systems, Inc.

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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