Marion Laboratories, Inc.
Marion Laboratories, Inc. holds FDA 510(k) medical device clearances, first cleared 1978, most recent 1989.
Top product codes for Marion Laboratories, Inc.
Recent clearances by Marion Laboratories, Inc.
- K883391 — POLYMER ADHESIVE BANDAGE
- K875182 — MODIFIED LABELING FOR TOXI-LAB THC SCREEN
- K875181 — MODIFIED LABELING FOR TOXI-LAB BROAD SPECTRUM
- K874554 — ENVICLUSIVE (TM)
- K874551 — ENVINET(TM)
- K874552 — ENVISAN PAD
- K874553 — ENVISAN PASTE
- K870864 — CULTURETTE BRAND CDT CLOSTRIDIUM DIFFICILE TEST
- K863485 — MODIFICATION OF CDT(TM) CLOSTRIDIUM TEST
- K862123 — BIOSPHERE ANAEROBIC ENVIRONMENTAL DEVICE
- K853073 — CULTURETTE BRAND 10-MINUTE GROUP A STREP I.D.
- K852044 — CULTURETTE BRAND RAPID LATEX TEST CLOSTRIDIUM TOXI
- K851399 — BAC-T-SCREEN
- K845008 — BIO-BAG ENVIRONMENTAL CHAMBER -TYPE A-MULTI-PLATE
- K833917 — BAC-T-SCREEN
- K831456 — TOXI-LAB CANNABINOID THC SCREEN
- K830372 — ARTIMICROBIAL REMOVAL DEVICE
- K823850 — BAC-T-SCREEN BACTERIURIA DETECTION DEV
- K823523 — TOXI-LAB RAPID SCREEN
- K822344 — ANTIMICROBIAL REMOVAL DEVICE (ARD)
- K812919 — MULTI-GRAM DEVELOPING TANK R-12 & R-3
- K811067 — BIO-BAG TM ENVIRONMENTAL CHAMBER TYPE M
- K810613 — ANTIMICROBIAL REMOVAL DEVICE
- K803298 — MINI-TIP CULTURETTE
- K802319 — HEMOTEMP TM
- K800052 — ANTIMICROBIAL REMOVAL DEVICE (ARD)
- K792654 — CULTURETTE BRAND-PVA/FORMALIN KIT
- K791724 — BIO-BAG ENVIRONMENTAL CHAMBER (A & B)
- K790815 — CULTURETTE BRAND PVA
- K790265 — LEVO-STAND-UP WHEELCHAIR
- K782016 — SPIROCARE 108-B
- K781868 — DROPPER, CEPTI-SEAL LAVTOPHENOL
- K781869 — DROPPER, CEPTI-SEAL KOH SOLUTION
- K781061 — DROPPERS, SOLUTION, IODINE
- K781062 — DROPPER, SOLUTION TRICHROME, CEPTI-SEAL
- K780440 — CHAMBER, AEROBIC
- K780222 — I.V. START KIT
- K780346 — MIF PROCEDURE KIT
Data sourced from openFDA. This site is unofficial and independent of the FDA.