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

LOPEZ-HORN CARRIER

K Number: K831312 · Decision May 25, 1983
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
3
Applicant Total
34
Review Days
33

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
LOPEZ-HORN CARRIER
K Number
K831312
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5740
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Chiron Vision Corp.
Date Received
April 22, 1983
Decision Date
May 25, 1983
Product Code
KYP
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
KYP Snake Bite Suction Kit

Similar 510(k) Clearances

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

View all

Other Clearances by Chiron Vision Corp.

K Number Device Name
K970727 MPORT FOLDABLE LENS PLACEMENT SYSTEM
K972808 HANSATOME MICROKERATOME
K960414 SYNERGIST POWER PACK
K944993 IOLAB.SITE CD PHACOEMULSIFICATION MODULE
K944995 IOLAB/SITE PERISTALTIC MODULE
K951292 PASSPORT FOLDABLE LENS PLACEMENT SYSTEM
K944994 IOLAB/SITE DISPOSABLE DIAPHRAGM CASSETTE
K941550 AUTOMATIC CORNEAL SHAPER SURGICAL INSTRUMENT
K935233 IOLAB LACRIMAL DUCT CATHETER
K925606 OPTICAL ZONE/HEXAGONAL/ASTIGMATISM/RADIAL MARKERS
Search all 34 clearances from Chiron Vision Corp. →