FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

3I MODEL(S)7426 AND 7427 CELSEP CENTRIFUGE SYSTEM

K Number: K994148 · Decision Feb 1, 2000
Classifications
1
FEI Numbers
163
Registration Numbers
163
Same Product Code
37
Applicant Total
51
Review Days
55

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Basic Information

Device Name
3I MODEL(S)7426 AND 7427 CELSEP CENTRIFUGE SYSTEM
K Number
K994148
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.2050
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Implant Innovations, Inc.
Date Received
December 8, 1999
Decision Date
February 1, 2000
Product Code
JQC
Advisory Committee
Clinical Chemistry
Review Advisory Committee
IM
Third Party
N

Classifications

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

Product Code Device Name
JQC Centrifuges (Micro, Ultra, Refrigerated) For Clinical Use

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Other Clearances by Implant Innovations, Inc.

K Number Device Name
K062636 OSSEOTITE, OSSEOTITE NY, CERTAIN, CERTAIN NT, PREVAIL, CERTAIN PREVAIL, XP, MICROMINIPLANT, DENTAL IMPLANTS
K063341 3I OSSEOTITE CERTAIN DENTAL IMPLANTS
K063286 OSSEOTITE; OSSEOTITE NT; XP; TG OSSEOTITE
K063403 CONICAL ANGLED ABUTMENT
K061629 CERTAIN PREVAIL DENTAL IMPLANT
K062432 NANOTITE DENTAL IMPLANTS
K061969 PREFORMANCE POSTS AND TEMPORARY CYLINDERS
K061177 PROVIDE TEMPORARY CYLINDER
K060291 PREFORMANCE TEMPORARY CYLINDER
K053170 PREFORMANCE POSTS
Search all 51 clearances from Implant Innovations, Inc. →