Procedure Products, Inc.
Procedure Products, Inc. holds FDA 510(k) medical device clearances, first cleared 1981, most recent 2017, with 1 FDA device recall on record.
Top product codes for Procedure Products, Inc.
FDA recalls by Procedure Products, Inc.
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 Procedure Products, Inc.
- K161812 — Freedom Syringe
- K923194 — INSUFFLATOR CONNECTING FILTER
- K922536 — TORQUE DEVICE
- K914128 — CONNECTING SET
- K910673 — BAG SPIGOT
- K884985 — MODIFIED 10CC SYRINGE CONTROL RING SET
- K874747 — 10CC SYRINGE CONTROL RING SET
- K874037 — ANGIO WASTE FLUIDS DUMP BAG
- K853749 — CUSTOM CORONARY MANIFOLD KITS
- K842173 — DISPOSABLE STOPCOCKS
- K833554 — MATERIAL ADDITION LEXAN & K-RESIN
- K820384 — GLASS SYRINGES, DRUG, LUER LOCK
- K812657 — INJECTION CAP, LUER LOCK
- K811548 — CERVICAL SPATULA
- K810921 — MALE LUER LOCK PLUGS
- K810859 — SINGLE USE SELDINGER/COURNAND PERC. NDL
Data sourced from openFDA. This site is unofficial and independent of the FDA.