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

OPERAND* LUBRICATING JELLY

K Number: K900110 · Decision May 2, 1990
Classifications
1
FEI Numbers
115
Registration Numbers
115
Same Product Code
48
Applicant Total
15
Review Days
113

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Basic Information

Device Name
OPERAND* LUBRICATING JELLY
K Number
K900110
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6375
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
General Medical Co.
Date Received
January 9, 1990
Decision Date
May 2, 1990
Product Code
KMJ
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
KMJ Lubricant, Patient

Similar 510(k) Clearances

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Other Clearances by General Medical Co.

K Number Device Name
K926269 PROCEDURE KIT
K912975 OPERAND LUBRICATING JELLY
K912132 OPERAND LUBRICATING JELLY
K903669 GENESIS INSUFFLATING CATHETER
K853635 SUBDERM TM
K844652 C.A.S.E. CONTAINER
K831320 DRIONIC
K820689 C.S.R. WRAPPERS
K820521 STERILIZATION WRAP
K802231 AIR VIVA II
Search all 15 clearances from General Medical Co. →