Louis M. Gerson Co., Inc.
Louis M. Gerson Co., Inc. holds FDA 510(k) medical device clearances, first cleared 1980, most recent 2006.
Top product codes for Louis M. Gerson Co., Inc.
Recent clearances by Louis M. Gerson Co., Inc.
- K061375 — RESPIRATOR N95 PARTICULATE RESPIRATOR, MODEL 1730
- K050193 — GERSON 2130/31 TYPE N95 NIOSH CERTIFIED SURGICAL RESPIRATOR
- K960778 — ISOLAIR APR TYPE N95
- K925185 — ISOLAIR 2 FLUID RESIST SURG/PROCE/CONE/EARLOOP MAS
- K931288 — ISOLAIR 2 FULL FACE SPLASH GUARD
- K922507 — GERSON ISOLAIR APR PARTICULATE SURGICAL MASK
- K881910 — LABELING CHANGE TO SURGICAL FACE MASK
- K802373 — SURGICAL FACE MASK
Data sourced from openFDA. This site is unofficial and independent of the FDA.