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

MEDI-PAK LEMON GLYCEOIN SWABS

K Number: K770583 · Decision May 26, 1977
Classifications
1
FEI Numbers
364
Registration Numbers
364
Same Product Code
20
Applicant Total
15
Review Days
59

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Basic Information

Device Name
MEDI-PAK LEMON GLYCEOIN SWABS
K Number
K770583
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6025
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
General Medical Co.
Date Received
March 28, 1977
Decision Date
May 26, 1977
Product Code
KXF
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
KXF Applicator, Absorbent Tipped, Non-Sterile

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
K900110 OPERAND* LUBRICATING JELLY
K853635 SUBDERM TM
K844652 C.A.S.E. CONTAINER
K831320 DRIONIC
K820689 C.S.R. WRAPPERS
K820521 STERILIZATION WRAP
Search all 15 clearances from General Medical Co. →