Search F2 TechNotes
Categories
- ASCA Program
- ATEX Directive 2014/34/EU
- Batteries
- CE marking
- Consulting
- EMC Directive 2014/30/EU
- EMC Testing
- EN 60601-1
- EU Battery Regulation (EU)2023/152
- EVs
- FCC
- FDA
- Field Label
- General Product Safety Directive 2001/95/EC
- General Product Safety Regulation (EU) 2023/988
- GPSR
- GPSR (EU)2023/988
- IEC 60601-1-9
- International Testing
- IP Testing
- Lasers
- Listing
- Low Voltage Directive 2014/35/EU
- Machinery Directive 2006/42/EC
- Machinery Regulation (EU)2023/1230
- Medical Devices Regulation (EU)2017/745
- PPE Regulation (EU) 2016/425
- Pressure Equipment Directive 2014/68/EU
- Product Testing
- Prop 65
- R&TTE Directive 1999/5/EC
- Radio Equipment Directive 2014/53/EU
- REACH
- RoHS Directive 2011/65/EU
- SPE-1000
- UKCA
- UL 4200A
- UL 60335-1
- UL 61010-1
- UL 62368-1
- UL 94
- US Field Label
-
Recent Posts
June 2025 M T W T F S S 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30
Tag Archives: medical device testing
The FDA’s ASCA Program and What it Means
This is the first time in history that the FDA has had a list of approved labs. F2 Labs is officially an ASCA-accredited testing laboratory. Continue reading
Posted in ASCA Program, FCC, FDA
Tagged ASCA, FDA, Medical Device, medical device testing
Comments Off on The FDA’s ASCA Program and What it Means