FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

AO NON-CONTACT II TONOMETER

K Number: K802419 · Decision Nov 12, 1980
Classifications
1
FEI Numbers
36
Registration Numbers
37
Same Product Code
57
Applicant Total
35
Review Days
37

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
AO NON-CONTACT II TONOMETER
K Number
K802419
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.1930
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Applicant
American Optical Corp.
Date Received
October 6, 1980
Decision Date
November 12, 1980
Product Code
HKX
Advisory Committee
Ophthalmic
Review Advisory Committee
OP
Third Party
N

Classifications

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

Product Code Device Name
HKX Tonometer, Ac-Powered

Similar 510(k) Clearances

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

View all

Other Clearances by American Optical Corp.

K Number Device Name
K950881 PHACO TIP
K950880 AOI UNIVERSAL ULTRASONIC HANDPIECE
K931358 AORP4000 REUSABLE PAK
K931354 P4000 PHACOEMULSIFIER
K931357 AOD4000 DISPOSABLE PAK
K820790 FLEXIBLE PROCTOSIGMOIDOSCOPE, #FPS-3
K813430 TISSUE PROCESSING CASSETTES & ACCESS
K812965 MODEL SC-6, FLEXIBLE SIAMOIDOSCOPE
K812051 PHOTOLITE AOLITE TINTOMATIC LENS
K812063 SR-1V DATA PRINTER
Search all 35 clearances from American Optical Corp. →