Dlp, Inc.
FDA 510(k) & PMA Approved Devices — 56 products
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Total Devices56
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K973485 | CLEARVIEW BLOWER/MISTER | FQH | 1997-12-08 | View |
| 510(k) | K964445 | OCTOPUS TISSUE STABILIZER (28001/28002/28003/28004/28005/28006) | DWS | 1997-01-30 | View |
| 510(k) | K953945 | RETROGRADE CORONARY SINUS PERFUSION CANNULA WITH ELONGATED & TREADED CUFF & INTRODUCER STYLET | DWF | 1996-03-26 | View |
| 510(k) | K950754 | MACRO SUCTION TUBE MODEL NO 10061 | GCY | 1995-04-25 | View |
| 510(k) | K934215 | CONTAIN-OR | KKX | 1994-02-09 | View |
| 510(k) | K915268 | CATHETER TWO STAGE VENOUS RETURN | DWF | 1992-07-27 | View |
| 510(k) | K913077 | LANCASTER COOLING JACKET, CAT. CODE #13500/13501 | DTR | 1992-01-09 | View |
| 510(k) | K914608 | BREAST LES LOCAL WIRE ST. 48219/49220/48119/48120 | GAA | 1992-01-09 | View |
| 510(k) | K913098 | APIRATION BIOPSY SYRINGE GUN, CAT. CODE #54501 | KNW | 1991-11-05 | View |
| 510(k) | K912229 | IMA ELECTROCAUTERY ELECTRODE CAT. #60002/60003 | GEI | 1991-09-25 | View |
| 510(k) | K904172 | ACCUPLACE (TM) | GDF | 1990-11-21 | View |
| 510(k) | K900994 | ANTEGRADE/RETROGRADE Y W/INTEGRAL SELECTOR SWIT. | DTL | 1990-08-15 | View |
| 510(k) | K901074 | CODE #94315 RETROGRADE CORONARY SINUS PERF CANNULA | DWF | 1990-07-06 | View |
| 510(k) | K900082 | MAXX 470 CORE BIOPSY GUN | KNW | 1990-06-27 | View |
| 510(k) | K897022 | PICSO CANNULA, CATALOG CODE 94315 | DWF | 1990-03-16 | View |
| 510(k) | K896019 | MODIFIED DISP. CHIBA-TYPE NEEDLE DESIGNATED ASPI. | GAA | 1990-01-03 | View |
| 510(k) | K893418 | MYOCARDIAL PROBE THERMOMETER CODE 64000 | FLL | 1989-09-05 | View |
| 510(k) | K891537 | CORE BIOPSY NEEDLE, CATALOG CODE #54006 | GDM | 1989-04-18 | View |
| 510(k) | K890707 | PHRENIC NERVE PAD & NERVE PAD W/1/4 PERCARDIAL | DWS | 1989-04-10 | View |
| 510(k) | K890453 | REUSABLE MLYOCARDIAL BIOPSY FORCEPS (BIOPTOMES | DWZ | 1989-03-31 | View |
No matching devices.
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