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FDA 510(k)

JJ SKINNER CAREKITS(TM) DRY/WET/GEL SKIN SCRUB KIT

K-Number: K925467 · 1994-05-11

ApplicantJ.J. Skinner, Inc.
Decision Date1994-05-11
Product CodeLRO
Advisory CommitteeSU
DecisionUnknown

Device Summary

JJ SKINNER CAREKITS(TM) DRY/WET/GEL SKIN SCRUB 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 1994-05-11 under 510(k) number K925467. The device is classified under product code LRO. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the JJ SKINNER CAREKITS(TM) DRY/WET/GEL SKIN SCRUB KIT?

JJ SKINNER CAREKITS(TM) DRY/WET/GEL SKIN SCRUB KIT is a medical device that received FDA 510(k) clearance on 1994-05-11. The listed applicant is J.J. Skinner, Inc.. The 510(k) number is K925467.

When did JJ SKINNER CAREKITS(TM) DRY/WET/GEL SKIN SCRUB KIT receive FDA 510(k) clearance?

JJ SKINNER CAREKITS(TM) DRY/WET/GEL SKIN SCRUB KIT received FDA 510(k) clearance on 1994-05-11, under 510(k) number K925467.

Who is the listed applicant for JJ SKINNER CAREKITS(TM) DRY/WET/GEL SKIN SCRUB 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) DRY/WET/GEL SKIN SCRUB KIT?

The FDA product code for JJ SKINNER CAREKITS(TM) DRY/WET/GEL SKIN SCRUB KIT is LRO.

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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 KITK925468JJ SKINNER CAREKITS(TM) BLOOD COLLECTION KITK903545CAREKITS(TM), IV/CATH/CENT LINE DRESS/TPN/CVP KITSK903544CAREKITS(TM) INCISION/DRAINAGE/SUTURE REMOVAL KITS

View all 7 devices →

Related Devices (Code: LRO)

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.

K213481Medline General Surgery TrayMedline Industries, Inc.K212258Medline Cardiovascular Procedure KitMedline Industries, Inc.K041080SURGICAL DRAPE KIT - D.I.R.R.A. SRLD.I.R.R.A. S.R.L.K030721QUICK-TAP PARACENTESIS TRAY, KIT & NEEDLEBallard Medical ProductsK023276AMSINO TRACHEOSTOMY CARE TRAYAmsino International, Inc.K980137WORLDWIDE MEDICAL TECHNOLOGIES BONE MARROW BIOPSY PROCEDURE TRAYWorldwide Medical Technologies, LLC

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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