EYE TRAY— 510(k) K940239

Unknown

Cush Medical Products

FDA 510(k) clearance K940239 for EYE TRAY, Unknown on 1994-06-28. Applicant: Cush Medical Products. Device class: 1.

Clearance details

Applicant: Cush Medical Products
Product code: Code LRP
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1994-01-19
Decision date: 1994-06-28
Decision: Unknown
Clearance type: Traditional
Location: Piney Flats, TN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LRP

K963723 — LACERATION TRAY1996-11-27
K951811 — OSTEOTECH MUSCULOSKELETAL TISSUE RECOVERY PACK1995-05-31
K935621 — CUSTOM ENT PACKS1994-03-30
K940646 — ORTHOPEDIC TRAY PRODUCT LINE1994-03-11
K940444 — GENERAL SURGERY TRAY1994-03-07

More clearances from Cush Medical Products

K943424 — CUSH ISLAND DRESSING1994-10-03
K940518 — C-SECTION TRAY1994-08-18
K941349 — DENTAL TRAY1994-07-26
K941645 — BIOPSY TRAY1994-07-14
K935684 — IV START KIT1994-06-10

Data sourced from openFDA. This site is unofficial and independent of the FDA.