FDA.report

510(k) K810530

Device
PERI-PATCH GLUE MOLD
Applicant
QUINTON, INC.
510(k) number
K810530
Product code
KGZ  
Decision
Substantially Equivalent (SESE)
Decision date
1981-03-24
Date received
1981-02-26
Regulation
878.4200
Classification name
Accessories, Catheter
Medical specialty
General & Plastic Surgery
Review panel
General & Plastic Surgery
Device class
1
Clearance type
Traditional
Third party reviewed
No
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Address
803 N. Front St. Suite 3 Mchenry IL US 60050 60050

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF not indicated by FDA · openFDA JSON

Other 510(k) Records For Product Code KGZ  

510(k)DeviceApplicantDecision date
K022306AART SILICONE TUBINGAesthetic and Reconstructive Technologies, Inc.2002-10-10
K974295BYRON MEDICAL ASPIRATION AND INFILTRATION/IRRIGATION TUBINGByron Medical1998-02-10
K973183WOUND DRAINAGE HOLDERR & D Medical Products, Inc.1998-01-23
K955433DURALASTIC SILICONE TUBINGAllied Biomedical Corp.1996-01-26
K942315NAVARRE PERCUTANEOUS ACCESS SETNavarre Biomedical , Ltd.1994-07-08
K896087PALESTRANT IRRIGATION AND DRAINAGE SETNorth American Instrument Corp.1989-11-03
K895041OPTICAL CATHETER(TM) INTRODUCER SETSMedical Dynamics, Inc.1989-10-16
K893406DESERET PRN ADAPTERDeseret Medical, Inc.1989-06-22
K873009CONCEPT SWITCHING STICKConcept, Inc.1987-08-17
K870014HCI GENERAL PURPOSE CATHETER STYLETHealth Care Innovations, Inc.1987-02-06
K864115TUBEGRIPPER, DRAINAGE CATHETER & ACCESSORY FOR SUCathaid, Inc.1986-11-07
K855078ANGIO MED DISPOSABLE PRESSURE CONNECTORSAngiomed U.S., Inc.1986-02-19
K842666NU-THOR THORACOSTOMY KITIntl. Medical Devices , Ltd.1984-09-20
K821525DESERET UNIVERSAL LUER LOCKWarner-Lambert Co.1982-06-23
K821245DESERET OFFSET PRN ADAPTERWarner-Lambert Co.1982-05-13

Legacy Summary

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FDA Review

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