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FDA 510(k)

INTERMITTENT INJECTION SITE

K-Number: K923323 · 1993-07-13

ApplicantKawasumi Laboratories Co., Ltd.
Decision Date1993-07-13
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INTERMITTENT INJECTION SITE is the device name listed in this FDA 510(k) record. The listed applicant is Kawasumi Laboratories Co., Ltd.. It received FDA 510(k) clearance on 1993-07-13 under 510(k) number K923323. 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 INTERMITTENT INJECTION SITE?

INTERMITTENT INJECTION SITE is a medical device that received FDA 510(k) clearance on 1993-07-13. The listed applicant is Kawasumi Laboratories Co., Ltd.. The 510(k) number is K923323.

When did INTERMITTENT INJECTION SITE receive FDA 510(k) clearance?

INTERMITTENT INJECTION SITE received FDA 510(k) clearance on 1993-07-13, under 510(k) number K923323.

Who is the listed applicant for INTERMITTENT INJECTION SITE?

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

What is the FDA product code for INTERMITTENT INJECTION SITE?

The FDA product code for INTERMITTENT INJECTION SITE is FOZ.

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Other records listing Kawasumi Laboratories Co., Ltd. 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.

K994323KAWASUMI LABORATORIES PHILEBOTOMY SETK974829NON-PVC FLUID PATH PORT ACCESS INFUSION SET (WITH AND WITHOUT INJECTION SET)K964117NON-PVC FLUID PATH PORT ACCESS INFUSION SET WITH SLIT SEPTUM INJECTION SITEK935514VACUUM TUBE HOLDER CULTURE MEDIUM VIAL HOLDERK935505WINGED COLLECTION SET W/MULTI-SAMPLE LUER ADAPTERK935506MULTI-SAMPLE LUER ADAPTER FOR BLOOD SAMPLE COLLECTION

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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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