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

SAPPHIRE LINE FLAT DRAIN/KIT WITH SPI-ARGENT II W/OR W/OUT TROCAR

K Number: K961295 · Decision Jun 26, 1996
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
76
Applicant Total
29
Review Days
83

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Basic Information

Device Name
SAPPHIRE LINE FLAT DRAIN/KIT WITH SPI-ARGENT II W/OR W/OUT TROCAR
K Number
K961295
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Sil-Med Corp.
Date Received
April 4, 1996
Decision Date
June 26, 1996
Product Code
GBX
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
GBX Catheter, Irrigation

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Other Clearances by Sil-Med Corp.

K Number Device Name
K972521 NAVIGATOR (STYLET) 2006
K961392 ANTIMICROBIAL PERITONEAL DIALYSIS COIL CATHETER WITH SPI-ARGENT II
K961194 ANTIMICROBIAL MEDIASTINAL SILICONE DRAIN
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
K921424 SIL-MED FLAT SUCTION DRAIN
Search all 29 clearances from Sil-Med Corp. →