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

CANNULAS FOR HEMA-TEK I & KK SLIDE STAINERS

K Number: K850157 · Decision Feb 27, 1985
Classifications
1
FEI Numbers
82
Registration Numbers
82
Same Product Code
20
Applicant Total
35
Review Days
43

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Basic Information

Device Name
CANNULAS FOR HEMA-TEK I & KK SLIDE STAINERS
K Number
K850157
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.3800
Medical Specialty
Pathology
Decision
Substantially Equivalent
Applicant
Shaban Mfg. Co.
Date Received
January 15, 1985
Decision Date
February 27, 1985
Product Code
KPA
Advisory Committee
Pathology
Review Advisory Committee
HE
Third Party
N

Classifications

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

Product Code Device Name
KPA Slide Stainer, Automated

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Other Clearances by Shaban Mfg. Co.

K Number Device Name
K853621 REPLACEMENT PUMP TUBING
K850333 PUMP TUBE SETS FOR HEMA-TEK I & II SLIDE STAINERS
K844781 MEMBRANE KITS-KC1, CO2 & 02 FOR INSTRUMENT-LAB
K844235 CHLORIDE STANDARD
K842656 REPLACEMENT PARTS NOVA ELECTROLYTE ANAL
K841610 COMPONENTS FOR POTASSIUM, SODIUM CHLO
K841609 COMPONENTS FOR PARTIAL PRESSURE ELEE
K840557 REAGENTS & STANDARDS IL 501 NA/K
K840468 PARTIAL PRESS. ELECTRODE MEASUREMENT
K840530 SUPPLIES FOR INSTRUMENTATION LAB FLAME
Search all 35 clearances from Shaban Mfg. Co. →