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

I/A KIT

K Number: K830859 · Decision May 2, 1983
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
76
Applicant Total
10
Review Days
46

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Basic Information

Device Name
I/A KIT
K Number
K830859
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Surgeon Surgical Instrumentation, Inc.
Date Received
March 17, 1983
Decision Date
May 2, 1983
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GBX), ordered by most recent decision date.

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Other Clearances by Surgeon Surgical Instrumentation, Inc.

K Number Device Name
K954241 SURGIN GENISIS PHACOEMULSIFIER
K932281 VERRES NEEDLE
K922038 CO2 INSUFFLATION TUBING
K904010 SURGICAL ASPIRATOR KIT
K890447 HEMORRHAGE OCCLUDOR
K880543 UNI-PORT
K881232 SURGIN EYE SHIELD
K861203 MULTI-SPIKE
K852229 STERILE EYE PACKS OR TRAYS