FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DISPOSABLE BLOOD LINE CONNECTORS

K Number: K821495 · Decision May 27, 1982
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
181
Applicant Total
55
Review Days
8

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Basic Information

Device Name
DISPOSABLE BLOOD LINE CONNECTORS
K Number
K821495
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5820
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Bentley Laboratories, Inc.
Date Received
May 19, 1982
Decision Date
May 27, 1982
Product Code
KOC
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
HE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KOC Accessories, Blood Circuit, Hemodialysis

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K903641 QUICK PRIME HEMOCONCEN. NO. HQ-7000 AND CBP-7000Q
K894826 UNIVOX W/HOLDERS, MODELS UNIVOX-HL, HLB, HLF
K874841 INTEGRATED MEMBRANE OXYGENATOR W/CARDIOTOMY FILTER
K874867 CATR(TM)-H CARDIOTOMY HOLDER
K874618 BAXTER ACCUPORT(TM) CENTRAL VENOUS CATHETER
K823273 BOS-2S, SPIRAFLO BUBBLE INFANT OXYGEN.
K823359 OXYGEN CONSUMPTION MONITOR #OCM-0100
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