MEGA LUMBAR PUNCTURE KIT— 510(k) K910089
UnknownMegadyne Medical Products, Inc.
FDA 510(k) clearance K910089 for MEGA LUMBAR PUNCTURE KIT, Unknown on 1991-06-20. Applicant: Megadyne Medical Products, Inc.. Device class: 2.
Clearance details
- Applicant
- Megadyne Medical Products, Inc.
- Product code
- Code FMJ
- Device class
- Class 2
- Regulation
- 21 CFR 880.2500
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Traditional
- Location
- Tampa, FL, US
Recent devices under product code FMJ
view allMore clearances from Megadyne Medical Products, Inc.
view all- K233644 — Megadyne Patient Return Electrode Pad - Universal Dual (model 0846), Megadyne Patient Return Electrode Pad - Universal Plus (model 0847), Megadyne Patient Return Electrode Pad - Universal Dual Plus (model 0848)
- K213696 — ETHICON Megadyne Electrosurgical Generator
- K200250 — Megadyne Smoke Evacuator, Megadyne Filter, Megadyne Fluid Trap, Megadyne Connect Cable, 1 m and 2.1 m, Megadyne RF Sensor
- K193145 — Ethicon Megadyne Electrosurgical Generator, Bipolar Footswitch
- K191328 — Megadyne Foot Switch
Data sourced from openFDA. This site is unofficial and independent of the FDA.