Excelsior Medical Corp.
Excelsior Medical Corp. holds FDA 510(k) medical device clearances, first cleared 1995, most recent 2013, with 2 FDA device recalls on record.
Top product codes for Excelsior Medical Corp.
FDA recalls by Excelsior Medical Corp.
- Z-1989-2016 — Excelsior Disposable Syringe Heparin Lock Flush, USP syringe (5 mL Fill in 10 mL syringe). For flushing of IV catheters and IV tubing only.
- Z-2070-2014 — Excelsior Medical Sterile Triple Lead Tubing Set and Sterile Heavy Duty Triple Lead Tubing Set. To be used with the Pharm-Assist Dispensing Pump. Used for drug reconstitution and/or fluid transfer
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 Excelsior Medical Corp.
- K130975 — SWABCAP AND SWABFLUSH
- K101270 — SWABFLSUH (3ML, 5ML, 10ML) MODEL 10331, 10351, 10311
- K083508 — SWABCAP
- K082837 — STERILE FIELD SALINE PRE-FILLED SYRINGE(S)
- K061497 — SYREX HEPARIN LOCK FLUSH SYRINGE, 1 UNIT/ML & 2 UNITS/ML
- K053120 — STERILE FIELD SALINE AND HEPARIN LOCK FLUSH SYRINGES
- K023740 — SYREX PRE-FILLED SYRINGE
- K962938 — EXCELSIOR DISPOSABLE SYRINGE W/NORMAL SALINE (.9% SODIUM CHLORIDE)
- K942349 — MICROBORE EXTENSION SET
Data sourced from openFDA. This site is unofficial and independent of the FDA.