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U.S. Department of Health and Human Services

510(k) Premarket Notification
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81 to 90 of 491 Results
ProductCode: FOZ Decision Date To: 01/23/2022
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Device Name
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510(K)
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deseret arterial catheter PARKE-DAVIS CO. K851327 06/14/1985
no. 5300-3 1/2 french umbilical vessel cath. etc. SUPERIOR PLASTIC PRODUCTS CORP. K851981 06/18/1985
telet-lex medical iv catheter placement Teleflex Medical, Inc. K851142 07/05/1985
jelco & cathlon iv striped iv catheters-radiopagul CRITIKON COMPANY,LLC K853701 10/17/1985
l-cath expando cath LUTHER MEDICAL PRODUCTS, INC. K853348 01/09/1986
terumo surflo etfe i.v. catheter TERUMO MEDICAL CORP. K854566 01/23/1986
viapic central line catheter PARKE-DAVIS CO. K860290 03/18/1986
brawn and groshong catheters CATHETER TECHNOLOGY CORP. K860256 03/28/1986
polycath-h catheter ABBOTT LABORATORIES K854308 04/07/1986
one time hyperal & catheter dressing change trays ACME UNITED CORP. K861015 04/22/1986
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