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

SAV-A-LIMB

K Number: K833872 · Decision Feb 4, 1984
Classifications
1
FEI Numbers
166
Registration Numbers
166
Same Product Code
3
Applicant Total
29
Review Days
88

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Basic Information

Device Name
SAV-A-LIMB
K Number
K833872
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6050
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Sil-Med Corp.
Date Received
November 8, 1983
Decision Date
February 4, 1984
Product Code
KYR
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
KYR Bag, Ice

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K Number Device Name
K972521 NAVIGATOR (STYLET) 2006
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K961194 ANTIMICROBIAL MEDIASTINAL SILICONE DRAIN
K961295 SAPPHIRE LINE FLAT DRAIN/KIT WITH SPI-ARGENT II W/OR W/OUT TROCAR
K960099 PENROSE DRAIN MODELS 6001 - 6007
K955463 GRIP-A-BOOTS
K942709 MEDIASTINAL SILICONE DRAINS
K926496 SIL-SLIP (COATED/REGULAR(NON-COATED)THORACIC DRAIN
K926408 SIL-SLIP FLAT SUCTION DRAIN
K926495 SIL-SLIP ROUND WOUND DRAIN (COATED)/BLUE STRIPE
Search all 29 clearances from Sil-Med Corp. →