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FDA 510(k)

CAREKITS(TM) INCISION/DRAINAGE/SUTURE REMOVAL KITS

K-Number: K903544 · 1990-08-31

ApplicantJ.J. Skinner, Inc.
Decision Date1990-08-31
Product CodeLRP
Advisory CommitteeSU
DecisionUnknown

Device Summary

CAREKITS(TM) INCISION/DRAINAGE/SUTURE REMOVAL KITS 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 1990-08-31 under 510(k) number K903544. The device is classified under product code LRP. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the CAREKITS(TM) INCISION/DRAINAGE/SUTURE REMOVAL KITS?

CAREKITS(TM) INCISION/DRAINAGE/SUTURE REMOVAL KITS is a medical device that received FDA 510(k) clearance on 1990-08-31. The listed applicant is J.J. Skinner, Inc.. The 510(k) number is K903544.

When did CAREKITS(TM) INCISION/DRAINAGE/SUTURE REMOVAL KITS receive FDA 510(k) clearance?

CAREKITS(TM) INCISION/DRAINAGE/SUTURE REMOVAL KITS received FDA 510(k) clearance on 1990-08-31, under 510(k) number K903544.

Who is the listed applicant for CAREKITS(TM) INCISION/DRAINAGE/SUTURE REMOVAL KITS?

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 CAREKITS(TM) INCISION/DRAINAGE/SUTURE REMOVAL KITS?

The FDA product code for CAREKITS(TM) INCISION/DRAINAGE/SUTURE REMOVAL KITS is LRP.

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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 KITK925468JJ SKINNER CAREKITS(TM) BLOOD COLLECTION KITK903545CAREKITS(TM), IV/CATH/CENT LINE DRESS/TPN/CVP KITS

View all 7 devices →

Related Devices (Code: LRP)

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.

K963723LACERATION TRAYGrand Medical ProductsK951811OSTEOTECH MUSCULOSKELETAL TISSUE RECOVERY PACKOsteotech, Inc.K940239EYE TRAYCush Medical ProductsK935621CUSTOM ENT PACKSAssociated MedicalK940646ORTHOPEDIC TRAY PRODUCT LINECushinduK940444GENERAL SURGERY TRAYCush Medical Products

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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