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

CUP, DISPOSABLE MEDICINE

K Number: K760517 · Decision Nov 12, 1976
Classifications
1
FEI Numbers
275
Registration Numbers
276
Same Product Code
10
Applicant Total
13
Review Days
79

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Basic Information

Device Name
CUP, DISPOSABLE MEDICINE
K Number
K760517
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6430
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Landmark Plastics
Date Received
August 25, 1976
Decision Date
November 12, 1976
Product Code
KYX
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
KYX Dispenser, Liquid Medication

Similar 510(k) Clearances

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

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Other Clearances by Landmark Plastics

K Number Device Name
K760496 CUP, DISPOSABLE SPECIMEN
K760493 DISH, SOAP
K760492 BASIN, LARGE OR SMALL
K760490 BEDPAN, GENERAL MEDICAL MEDI-PAK
K760552 THERMOMETER STAND AND DUST COVER
K760494 BASIN, ROUND WASH
K760497 TRAY, SERVICE
K760495 BASIN, RECTANGULAR WASH
K760548 CARAFE AND LINER
K760491 TUMBLER, GENERAL MEDICAL MEDI-PAK
Search all 13 clearances from Landmark Plastics →