Agilent Technologies
Agilent Technologies holds FDA 510(k) medical device clearances, first cleared 1982, most recent 2001, with 1 FDA device recall on record.
Top product codes for Agilent Technologies
FDA recalls by Agilent Technologies
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Agilent Technologies
- K010949 — 2010 PLUS HOLTER FOR WINDOWS
- K003940 — 2010 PLUS HOLTER FOR WINDOWS
- K003763 — 2010 PLUS HOLTER FOR WINDOWS
- K001308 — MODIFICATION TO ZYMED TELEMETRY SYSTEM, MODEL EASIVIEW
- K990093 — ZYMED TELEMETRY SYSTEM: MODEL EASIVIEW
- K980186 — ZYMED TELEMETRY SYSTEM
- K942781 — DIGITAL HOLTER RECORDER
- K930806 — ZYMED HOLTER SCANNER MODEL 2010
- K924672 — ZYMED TELEMETRY MONITOR MODEL T8010 (PRELIMINARY)
- K895208 — ZYMED MODEL 1610
- K841083 — QUIKPAGE ARRHYTHMIA REPORT GENERATOR
- K822970 — HOLTER RECORDER
- K822582 — QUIKPAGE SCANNER
Data sourced from openFDA. This site is unofficial and independent of the FDA.