Pdg Product Design Group, Inc.
Pdg Product Design Group, Inc. holds FDA 510(k) medical device clearances, first cleared 1996, most recent 2017, with 1 FDA device recall on record.
Top product codes for Pdg Product Design Group, Inc.
FDA recalls by Pdg Product Design Group, 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 Pdg Product Design Group, Inc.
- K163432 — Stellar LEAP
- K140023 — ELEVATION
- K063736 — FUZE MECHANICAL WHEELCHAIR, MODELS T20 AND T50
- K061475 — ASTROTILT MANUAL WHEELCHAIR
- K990557 — THE STELLAR TILT, MANUALLY OPERATED WHEELCHAIR
- K971389 — ECLIPSE 400 MANUALLY OPERATED WHEELCAIR
- K970311 — BENTLEY MANUALLY OPERATED WHEELCHAIR
- K961743 — ECLIPSE 600 MANUALLY OPERATED WHEELCHAIR
Data sourced from openFDA. This site is unofficial and independent of the FDA.