Medical Device Consultants, Inc.
North Attleboro, MA, US
Medical Device Consultants, Inc. appears in FDA device records in North Attleboro, MA. FDA records list 14 510(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
- 14
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 14 510(k) clearances for Medical Device Consultants, Inc. between 1982 and 2002. The busiest year on record is 1986, with 5. The most recent is 2002, with 1.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1982 | 1 |
| 1984 | 1 |
| 1985 | 1 |
| 1986 | 5 |
| 1987 | 1 |
| 1997 | 1 |
| 2000 | 2 |
| 2001 | 1 |
| 2002 | 1 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K022895 | ELCAM STOPCOCKS AND MANIFOLDS | FMG | Substantially Equivalent | |
| K002699 | PARIETEX COMPOSITE (PCO) MESH | FTL | Substantially Equivalent | |
| K002116 | S3 CARDIOPLEGIA CONTROL MODULE VERSION 2.0 | DTQ | Substantially Equivalent | |
| K000551 | IMAGE X-70 PLUS DENTAL X-RAY UNIT | EHD | Substantially Equivalent | |
| K974164 | SWISS LITHOCLAST MASTER HANDPIECE AND 3.2 MM PROBE | FFK | Substantially Equivalent | |
| K864282 | GLUCOSE TESTCARD USE W/ILEX PROMPT CLINICAL CH ANA | CGA | Substantially Equivalent | |
| K860122 | HEMOTEC ACT HIGH RANGE ACTIVATED CLOTTING TIME | JBP | Substantially Equivalent | |
| K860932 | ULTRASUN 1000 & 2000 SUNTANNING UNIT | FTC | Substantially Equivalent | |
| K860931 | ULTRASUN 3000 AND 5000 SUNTANNING UNIT | FTC | Substantially Equivalent | |
| K860930 | ULTRASUN 2500 SUNTANNING UNIT | FTC | Substantially Equivalent | |
| K860929 | ULTRASUN 4000 FT & 15000-8 SUNTANNING UNIT | FTC | Substantially Equivalent | |
| K853198 | ADDITIONAL HEMOTEC ACT COAGULATION CARTRIDGES | JPA | Substantially Equivalent | |
| K840449 | AMICON DIAFILTER 40. HEMOFILTER | KDI | Substantially Equivalent | |
| K821651 | E-Z UP ARTHERAPEDIC CHAIR | INN | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- JBPActivated Whole Blood Clotting Time
- INNChair, Adjustable, Mechanical
- DTQConsole, Heart-Lung Machine, Cardiopulmonary Bypass
- KDIDialyzer, High Permeability With Or Without Sealed Dialysate System
- CGAGlucose Oxidase, Glucose
- FTCLight, Ultraviolet, Dermatological
- FFKLithotriptor, Electro-Hydraulic
- FTLMesh, Surgical, Polymeric
- FMGStopcock, I.V. Set
- JPASystem, Multipurpose For In Vitro Coagulation Studies
- EHDUnit, X-Ray, Extraoral With Timer
Recall records
No recall records for this company in the ingested FDA data.
Verification record
There is no verification record for this company. Most companies on this site have none: a record exists only where a company asked to be verified and MDM ran the checks, so the absence of one says nothing about the company.
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Data as of , FDA export datePage updated Source: openFDA, public domain