FDA 510(k) FDA class 2 Substantially Equivalent 🇪🇸 Spain

BOBES TONOMETER

K Number: K945446 · Decision Jun 20, 1995
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
55
Applicant Total
3
Review Days
225

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
BOBES TONOMETER
K Number
K945446
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
886.1930
Medical Specialty
Ophthalmic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Bobes S.A.
Date Received
November 7, 1994
Decision Date
June 20, 1995
Product Code
HKY
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
HKY Tonometer, Manual

Similar 510(k) Clearances

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

View all

Other Clearances by Bobes S.A.

K Number Device Name
K945445 BOBES SLIT LAMP
K945443 BOBES LENS SET