Hogan & Hartson
Hogan & Hartson holds FDA 510(k) medical device clearances, first cleared 1980, most recent 1998.
Top product codes for Hogan & Hartson
Recent clearances by Hogan & Hartson
- K974168 — COOPERSURGICAL INFRARED COAGULATOR
- K973849 — BIOABSORBABLE BANKART TACK
- K973162 — DUAL RADIATION TARGETING SYSTEM DRTS DRAPE
- K950169 — RIBOSOMAL P EIA TEST SYSTEM
- K942389 — TROCARS, TROCAR SLEEVES AND REDUCTION SLEEVES
- K946215 — CARDIOLIPIN G EIA TEST SYSTEM
- K946216 — CARDIOLIPIN A EIA TEST SYSTEM
- K946217 — CARDIOLIPIN M EIA TEST SYSTEM
- K946186 — CHAL-2500
- K941566 — COMPUSPEAK
- K946218 — MARDX ENA EIA TEST SYSTEM
- K950110 — MARDX MITOCHONDRIA EIA TEST SYSTEM
- K950836 — REDFIELD INFRARED COAGULATOR
- K942229 — MOTIVATOR FTR 2000
- K941762 — INTERGRATED MONITORING ARCHIVING AND COMMUNICATIONS SYSTEMS (IMACS)
- K946336 — MEGABEAM FIBER OPTIC DELIVERY SYSTEM
- K946101 — EMERGENCY/ACCIDENT TROLLEY 550
- K945161 — NORELCO CLEAN AIR SYSTEM CAS950
- K941417 — VITAFLON PLUS/VASCULON
- K942627 — 454A ELECTROSURGICAL ANALYZER
- K941404 — IMPULSE 4000 DEFIBRILLATOR/TRANSCUTANEOUS PACER ANALYZER
- K941819 — LIQUID OXYGEN STORAGE SUBSYSTEM
- K941909 — MEGA BEAM LATERAL FIRE
- K894973 — RESPITRACE PLUS
- K810045 — I.M. RETROGRADE BLADES
- K802951 — I.M PROBES
Data sourced from openFDA. This site is unofficial and independent of the FDA.