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

SPERM SELECT(TM)

K Number: K864524 · Decision Feb 2, 1987
Classifications
1
FEI Numbers
31
Registration Numbers
31
Same Product Code
258
Applicant Total
129
Review Days
77

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Basic Information

Device Name
SPERM SELECT(TM)
K Number
K864524
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.6180
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Pharmacia, Inc.
Date Received
November 17, 1986
Decision Date
February 2, 1987
Product Code
MQL
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
PA
Third Party
N

Classifications

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

Product Code Device Name
MQL Media, Reproductive

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K970420 MASTERCAP AM 5.0/MASTERCAP RM 5.0
K964152 UNICAP TOTAL IGE ASSAY/PHARMACIA TOTAL IGE CONTROLS LMH
K962274 UNICAP 100
K941993 PHARMACIA CAP SYSTEM PHADIATOP FEIA
K954337 GENOTROPIN MIXER
K951025 PISTON SYRINGE
K952025 ROBOCAP
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