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

SARNS MINI-SUCKER

K Number: K810416 · Decision Mar 5, 1981
Classifications
1
FEI Numbers
213
Registration Numbers
213
Same Product Code
95
Applicant Total
76
Review Days
15

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Basic Information

Device Name
SARNS MINI-SUCKER
K Number
K810416
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4680
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
3M Health Care, Sarns
Date Received
February 18, 1981
Decision Date
March 5, 1981
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

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Other Clearances by 3M Health Care, Sarns

K Number Device Name
K960916 SAMS 8000 CARDIOPLEGIA MONITOR
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K950739 3M SARNS FLOW SENSOR, CENTRIFUGAL CONTROL MODULE 115, 220 V, 900 PERFUSION SYSTEM
K941653 SARNS TURBO MEMBRANE OXYGENATOR MODIFICATION
K941654 SARNS FILTERED VENOUS RESERVIOR MODIFICATION
K940651 SARNS ULTRASONIC AIR SENSOR
K935391 SARNS STERNAL SAW II, STERNAL SAW II BLADE, SARNS SAW BLADES-NON-STERILE BULK PACK
K934127 SARNS LOW JETTING AORTIC ARCH CANNULA
K935977 SARNS AIR DETECTION SYSTEM
K915547 SARNS 8000 DELPHIN II CENTRI PUMP MOD W/INTEGR BAT
Search all 76 clearances from 3M Health Care, Sarns →