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FDA 510(k)

JJ SKINNER CAREKITS(TM) BLOOD COLLECTION KIT

K-Number: K925468 · 1994-04-11

ApplicantJ.J. Skinner, Inc.
Decision Date1994-04-11
Product CodeGJE
Advisory CommitteeCH
DecisionUnknown

Device Summary

JJ SKINNER CAREKITS(TM) BLOOD COLLECTION KIT is the device name listed in this FDA 510(k) record. The listed applicant is J.J. Skinner, Inc.. It received FDA 510(k) clearance on 1994-04-11 under 510(k) number K925468. The device is classified under product code GJE. It was reviewed by the CH advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the JJ SKINNER CAREKITS(TM) BLOOD COLLECTION KIT?

JJ SKINNER CAREKITS(TM) BLOOD COLLECTION KIT is a medical device that received FDA 510(k) clearance on 1994-04-11. The listed applicant is J.J. Skinner, Inc.. The 510(k) number is K925468.

When did JJ SKINNER CAREKITS(TM) BLOOD COLLECTION KIT receive FDA 510(k) clearance?

JJ SKINNER CAREKITS(TM) BLOOD COLLECTION KIT received FDA 510(k) clearance on 1994-04-11, under 510(k) number K925468.

Who is the listed applicant for JJ SKINNER CAREKITS(TM) BLOOD COLLECTION KIT?

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

What is the FDA product code for JJ SKINNER CAREKITS(TM) BLOOD COLLECTION KIT?

The FDA product code for JJ SKINNER CAREKITS(TM) BLOOD COLLECTION KIT is GJE.

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Other records listing J.J. Skinner, 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.

K961227JJ SKINNER CAREKITS WOUND CARE MANAGEMENT/DRESSING CHANGE TRAYK961683JJ SKINNER CAREKITS MINOR SURGICAL PROCEDURE TRAYK925469JJ SKINNER CAREKITS(TM) DIALYSIS ON/OFF KITK925467JJ SKINNER CAREKITS(TM) DRY/WET/GEL SKIN SCRUB KITK903545CAREKITS(TM), IV/CATH/CENT LINE DRESS/TPN/CVP KITSK903544CAREKITS(TM) INCISION/DRAINAGE/SUTURE REMOVAL KITS

View all 7 devices →

Related Devices (Code: GJE)

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.

K962596CUSTOMED BLOOD EXTRACTION KITCustomed, Inc.K780303AUTO ISO-FILTER COLLECTION TUBE CAPBd Becton Dickinson Vacutainer Systems PreanalyticK771489RTERIAL BLOOD SAMPLING KITBd Becton Dickinson Vacutainer Systems PreanalyticK771370ICROTAINEO BRAND TUBEBd Becton Dickinson Vacutainer Systems PreanalyticK761177SODIUM CITRATEBio/Data Corp.K760086TRAY, BLOOD SAMPLING (PULSATOR II)Concord Laboratories, 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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