Pharmaceutical Innovations, Inc.
Pharmaceutical Innovations, Inc. holds FDA 510(k) medical device clearances, first cleared 1996, most recent 2018, with 6 FDA device recalls on record.
Top product codes for Pharmaceutical Innovations, Inc.
FDA recalls by Pharmaceutical Innovations, Inc.
- Z-2830-2020 — Ultra/Phonic Focus BP Conforming Gel Pads, UDI 00300361301021 (Primary); 10300361301028 (Package) - Product Usage: A gel pad for use on woman s areola during an ultrasound examination. Its primary purpose is for patient comfort over the loose gel and helps with nipple location during the scan, making the areola location easier to identify.
- Z-1969-2019 — ElectroMist product codes: 36-3310-25 - Product Usage: Electrode conductivity spray solution.
- Z-1968-2019 — Alpha Conducting solution product codes:3310-15 ACS - Product Usage: Electrode conductivity spray solution.
- Z-1972-2019 — Alpha Conducting solution product codes: 3310-25 ASCR - Product Usage: Electrode Conductivity Spray Solution.
- Z-1971-2019 — ElectroMist product codes: 36-3310-04 - Product Usage: Electrode Conductivity Spray Solution.
- Z-1970-2019 — ElectroMist product codes: 36-3310-60 - Product Usage: Electrode Conductivity Spray Solution.
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 Pharmaceutical Innovations, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.