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

MTG - MINITUB HEATED STAGE SYSTEMS

K Number: K002971 · Decision Dec 15, 2000
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
45
Applicant Total
5
Review Days
84

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Basic Information

Device Name
MTG - MINITUB HEATED STAGE SYSTEMS
K Number
K002971
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.6120
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Zander Medical Supplies, Inc.
Date Received
September 22, 2000
Decision Date
December 15, 2000
Product Code
MQG
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

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

Product Code Device Name
MQG Accessory, Assisted Reproduction

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Other Clearances by Zander Medical Supplies, Inc.

K Number Device Name
K041952 ZIVF-AIRE
K011327 DB1 EMBRYO FREEZE
K002961 MINITUB MULTI-PURPOSE CASSETTES
K003184 RS BIOTECH GALAXY 'R' CO2 INCUBATOR