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

TURKEL ABDOMINAL PARACENTESIS SYSTEM

K Number: K924702 · Decision Jan 12, 1993
Classifications
1
FEI Numbers
243
Registration Numbers
243
Same Product Code
76
Applicant Total
34
Review Days
117

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Basic Information

Device Name
TURKEL ABDOMINAL PARACENTESIS SYSTEM
K Number
K924702
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4200
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Symbiosis Corp.
Date Received
September 17, 1992
Decision Date
January 12, 1993
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 Symbiosis Corp.

K Number Device Name
K955119 SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODES
K953453 SYMBIOSIS MONOPOLAR ELECTROSURGICAL ROLLER ELECTRODES
K953242 SYMBIOSIS MONOPLAR ELECTROSURGICAL ELECTRODES
K952432 SYMBIOSIS BIPOLAR FORCEPS
K951387 SYMBIOSIS BIPOLAR SCISSORS
K950286 SYMBIOSIS BIPOLAR SCISSORS
K946238 SYMBIOSIS GASTROINTESTINAL BIOPSY FORCEPS
K930773 SYMBIOSIS GYNECOLOGICAL BIOPSY FORCEPS
K941426 SYMBIOSIS REUSABLE MONOPOLAR ELECTROSURGICAL PROBE
K932266 SYMBIOSIS DISPOS GASTRO BIOPSY FORCEPS W/REUSE HAN
Search all 34 clearances from Symbiosis Corp. →