# K981432: Goldman Manual Tonometer

- Pathway: 510(k) (Traditional)
- Applicant: Golden Vision, Inc.
- Decided: Jan 12, 1999 after 267 days
- Product code: HKY (Tonometer, Manual)
- Device class: 2
- Regulation: 21 CFR 886.1930
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
25 later devices descend from it; 10 cite it directly.
0 of 26 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K021937: TGDC-01 Pra (2002), 11 descendants of its own
- K063873: Icare Tonometer TA01I (2007), 8 descendants of its own
- K093445: Keeler Applanation Tonometer; T-Type Kat, K-Type Kat, (Kat) (2010), 5 descendants of its own
- K153694: Icare ic100 (2016), 4 descendants of its own
- K133234: T-Type D-Kat, R-Type D-Kat (2014), 4 descendants of its own

## Indications for use
THE GOLDMAN MANUAL TONOMETER IS AN APPLIANCE THAT SERVES TO MEASURE INTRAOCULAR PRESSURE, ACCORDING TO THE GOLDMAN METHOD. THE MEASURING OF THE PRESSURE REQUIRES TO MAINTAIN A UNIFORM APPLANATION OF THE SURFACE OF THE CORNEA. IT IS SPECIALLY INDICATED IN GLAUCOMA DISEASE.

Source page: https://510kreport.com/device/K981432
Methodology: https://510kreport.com/methodology