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

DISP. YANKAVER SURG. SUCTION INSTRUMENT

K Number: K830123 · Decision Jun 8, 1983
Classifications
1
FEI Numbers
213
Registration Numbers
213
Same Product Code
95
Applicant Total
30
Review Days
148

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
DISP. YANKAVER SURG. SUCTION INSTRUMENT
K Number
K830123
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4680
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Narco Scientific
Date Received
January 11, 1983
Decision Date
June 8, 1983
Product Code
GCY
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
GCY Apparatus, Suction, Single Patient Use, Portable, Nonpowered

Similar 510(k) Clearances

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

View all

Other Clearances by Narco Scientific

K Number Device Name
K830338 NARCOTRACE 80
K831428 AS 1740 INTERFACE MODULE
K831429 AS 191 ECG TELEMETRY MODULE
K822835 PZ-800 VOLUME VENTILATOR
K831430 AIR SHIELDS AS-100 MONIORING SYS-AS105
K831460 AS 30/TCP MODULE
K831028 TI-1000 TRANSPORT INCUBATOR
K823899 INFANT CARE SYSTEM
K830680 AIR-SHIELDS VENTIMETER VENTILATOR-CONTR
K830654 INFUSION PUMP RETROGRADE EXTEN. AS 715
Search all 30 clearances from Narco Scientific →