PRINTER, DIGITAL
FDA 510(k) clearance K781115 · decided 1978-10-06
Clearance details
- K-number
- K781115
- Device name
- PRINTER, DIGITAL
- Applicant
- Output, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1978-07-03
- Decision date
- 1978-10-06
- Days to decision
- 95 days
- Clearance type
- Traditional
- Product code
- DSF
- Device class
- 1
- Regulation number
- 870.2810
- Medical specialty
- Cardiovascular
- Advisory committee
- Cardiovascular
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| EDENTEC DIGITAL CHARTER MODEL 3710 (K910871) | Edentec Corp. | 1991-08-29 |
| DASH IV (K912929) | Astro-Med, Inc. | 1991-08-13 |
| MODEL 556 MONITOR (K905856) | Ge Medical Systems Information Technologies | 1991-01-11 |
| GRI LASERGRAPH(TM) ECG PAPER (K902586) | Gri Medical Products, Inc. | 1990-06-22 |
| COLORADO COLOR IMAGING RECORDER (K902230) | Honeywell, Inc. | 1990-06-19 |
| GABRIEL MEDICAL CLS THERMAL RECORDER (K901385) | Gabriel Medical, Inc. | 1990-05-09 |
| TYPE 9541 RECORDER, PAPER CHART (K895111) | S & W Medico Teknik | 1990-01-26 |
| WR3500 AND WR3600 SERIES RECORDERS (K894922) | Western Graphtec | 1990-01-26 |
| MT96000 PAPER CHART RECORDER (K894736) | Astro-Med, Inc. | 1989-12-13 |
| PAQ10 PAPER CHART RECORDER (K894607) | Protocol Systems, Inc. | 1989-10-26 |
| EDENTRACE 670 SYSTEM MULTICHANNEL RECORDER W/OXIM. (K893561) | Edentec Corp. | 1989-08-25 |
| CARDIOCAP(TM) DR-104 REPORTER (K885058) | Datex Division Instrumentarium Corp. | 1989-07-14 |
Recalls involving this device
No recalls on record reference this clearance.