Hogan & Hartson
Mchenry, IL, US
Hogan & Hartson appears in FDA device records in Mchenry, IL. FDA records list 26 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 26
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 26 510(k) clearances for Hogan & Hartson between 1980 and 1998. The busiest year on record is 1995, with 9. The most recent is 1998, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1980 | 1 |
| 1981 | 1 |
| 1989 | 1 |
| 1994 | 6 |
| 1995 | 9 |
| 1996 | 5 |
| 1997 | 1 |
| 1998 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K974168 | COOPERSURGICAL INFRARED COAGULATOR | KNS | Substantially Equivalent | |
| K973849 | BIOABSORBABLE BANKART TACK | MAI | Substantially Equivalent | |
| K973162 | DUAL RADIATION TARGETING SYSTEM DRTS DRAPE | IWE | Substantially Equivalent | |
| K950169 | RIBOSOMAL P EIA TEST SYSTEM | MQA | Substantially Equivalent | |
| K942389 | TROCARS, TROCAR SLEEVES AND REDUCTION SLEEVES | HET | Substantially Equivalent | |
| K946217 | CARDIOLIPIN M EIA TEST SYSTEM | MID | Substantially Equivalent | |
| K946216 | CARDIOLIPIN A EIA TEST SYSTEM | MID | Substantially Equivalent | |
| K946215 | CARDIOLIPIN G EIA TEST SYSTEM | MID | Substantially Equivalent | |
| K946186 | CHAL-2500 | IPF | Substantially Equivalent for Some Indications | |
| K941566 | COMPUSPEAK | LLZ | Substantially Equivalent | |
| K950110 | MARDX MITOCHONDRIA EIA TEST SYSTEM | LJM | Substantially Equivalent | |
| K946218 | MARDX ENA EIA TEST SYSTEM | LJM | Substantially Equivalent | |
| K950836 | REDFIELD INFRARED COAGULATOR | KNS | Substantially Equivalent | |
| K942229 | MOTIVATOR FTR 2000 | IKK | Substantially Equivalent | |
| K941762 | INTERGRATED MONITORING ARCHIVING AND COMMUNICATIONS SYSTEMS (IMACS) | DQK | Substantially Equivalent | |
| K946336 | MEGABEAM FIBER OPTIC DELIVERY SYSTEM | GEX | Substantially Equivalent | |
| K946101 | EMERGENCY/ACCIDENT TROLLEY 550 | FPO | Substantially Equivalent | |
| K945161 | NORELCO CLEAN AIR SYSTEM CAS950 | FRF | Substantially Equivalent | |
| K941417 | VITAFLON PLUS/VASCULON | FOZ | Substantially Equivalent | |
| K942627 | 454A ELECTROSURGICAL ANALYZER | GEI | Substantially Equivalent | |
| K941404 | IMPULSE 4000 DEFIBRILLATOR/TRANSCUTANEOUS PACER ANALYZER | DRL | Substantially Equivalent | |
| K941909 | MEGA BEAM LATERAL FIRE | GEX | Substantially Equivalent | |
| K941819 | LIQUID OXYGEN STORAGE SUBSYSTEM | BYJ | Substantially Equivalent | |
| K894973 | RESPITRACE PLUS | FLS | Substantially Equivalent | |
| K810045 | I.M. RETROGRADE BLADES | GFA | Substantially Equivalent | |
| K802951 | I.M PROBES | HXB | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- MQAAnti-Ribosomal P Antibodies
- LJMAntinuclear Antibody (Enzyme-Labeled), Antigen, Controls
- GFABlade, Saw, General & Plastic Surgery, Surgical
- FOZCatheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
- FRFCleaner, Air, Medical Recirculating
- DQKComputer, Diagnostic, Programmable
- GEIElectrosurgical, Cutting & Coagulation & Accessories
- MAIFastener, Fixation, Biodegradable, Soft Tissue
- HETLaparoscope, Gynecologic (And Accessories)
- FLSMonitor, Apnea, Facility Use
- IWEMonitor, Patient Position, Light-Beam
- GEXPowered Laser Surgical Instrument
- HXBProbe
- IPFStimulator, Muscle, Powered
- FPOStretcher, Wheeled
- LLZSystem, Image Processing, Radiological
- IKKSystem, Isokinetic Testing And Evaluation
- MIDSystem, Test, Anticardiolipin Immunological
- DRLTester, Defibrillator
- KNSUnit, Electrosurgical, Endoscopic (With Or Without Accessories)
- BYJUnit, Liquid-Oxygen, Portable
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain