Contour Fabricators, Inc.
Contour Fabricators, Inc. holds FDA 510(k) medical device clearances, first cleared 1979, most recent 2009, with 1 FDA device recall on record.
Top product codes for Contour Fabricators, Inc.
FDA recalls by Contour Fabricators, 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 Contour Fabricators, Inc.
- K090773 — CFI ULTRASOUND PROBE DRAPE
- K970900 — INSTRUMENT HOLDER
- K971040 — CABLE HOLDER, SUCTION TUBE HOLDER
- K970185 — STERILE DISPOSABLE EQUIPMENT MAGNET COVER
- K964141 — GE STERILE DISPOSABLE EQUIPMENT COIL COVER
- K963453 — CFI RESTRAINT BELT (CFI-168) / CFI RESTRAINT BELT (CFI-4046)
- K820692 — BANDBAG, WRAP, STERILE
- K782155 — GENERAL EQUIPMENT COVER
Data sourced from openFDA. This site is unofficial and independent of the FDA.