Perkinelmer Life Sciences, Inc.
Perkinelmer Life Sciences, Inc. holds FDA 510(k) medical device clearance, cleared in 2004, with 2 FDA device recalls on record.
Top product codes for Perkinelmer Life Sciences, Inc.
FDA recalls by Perkinelmer Life Sciences, Inc.
- Z-0728-2018 — JANUS & JANUS G3 Automated Workstation is an automated programmable liquid handling instrument intended for use in clinical settings to facilitate the pipetting and dilution of solutions in sample preparation work flows.
- Z-2685-2017 — Multiphor II Electrophoresis System GE HealthCare Product Number: 18-1018-06 PerkinElmer Part Number: 2117-004 Product Usage: Multiphor II Electrophoresis System is a versatile modular electrophoresis system for horizontal electrophoresis, isoelectric focusing, 2-D electrophoresis and electrophoretic transfer Note: The Multiphor II Electrophoresis System (Class I) is the platform used with the hemoglobin electrophoresis gel kit ( Class II) sold by PerkinElmer as the Resolve Hemoglobin Kit (K050709: Product code JJN). The RESOLVE Systems Hemoglobin kit (K050709) is designed to separate whole blood, cord blood or dried blood spot specimen for detection of normal and variant hemoglobins by isoelectric focusing.
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 Perkinelmer Life Sciences, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.