NIDEK MODEL VT-4000, MODIFICATION
FDA 510(k) clearance K936302 · decided 1994-07-15
Clearance details
- K-number
- K936302
- Device name
- NIDEK MODEL VT-4000, MODIFICATION
- Applicant
- Nidek, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1993-12-29
- Decision date
- 1994-07-15
- Days to decision
- 198 days
- Clearance type
- Traditional
- Product code
- HQE
- Device class
- 2
- Regulation number
- 886.4150
- Medical specialty
- Ophthalmic
- Advisory committee
- Ophthalmic
- Location
- Fremont, CA, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Nidek
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| UniVit HE, UniVit UHS (K212763) | Visioncare Devices, LLC | 2022-08-10 |
| Cetus system, Cetus probe (K170183) | A.R.C Laser GmbH | 2017-09-27 |
| Bi-Blade Vitrectomy Cutter (K153168) | Medical Instrument Development Laboratories | 2016-04-29 |
| CONSTELLATION VISION SYSTEM (K141065) | Alcon Research, Ltd. | 2014-08-22 |
| VERSAVIT (K121675) | Synergetics, Inc. | 2012-06-21 |
| PROCARE PLUS VITRECTOMY SYSTEM (K120170) | Visioncare Devices, Inc. | 2012-05-30 |
| ULTIMATE VIT ENHAMCER (UVE) (K102222) | Medical Instrument Development Laboratories, Inc. | 2011-04-08 |
| COLIBRI DISPOSABLE VITRECTOMY CUTTER (K033390) | Microworld Medical Instruments, Inc. | 2003-11-04 |
| VMATE MODEL VMM1000 (K030948) | Howard Instruments, Inc. | 2003-06-17 |
| VELOCITY ADVANTAGE (K023939) | Visioncare Devices, Inc. | 2003-04-17 |
| MID LABS AUTONOMOUS VIT ENHANCER (AVE) (K020911) | Medical Instrument Development Laboratories, Inc. | 2002-04-29 |
| D.O.R.C. HARMONY TOTAL TTC VITRECTOMY SYSTEM (K010082) | Dutch Ophthalmic USA, Inc. | 2001-03-12 |
Recalls involving this device
No recalls on record reference this clearance.
PMA approvals by this applicant
| Record | Firm | Date |
|---|---|---|
| ND:YAG POSTERIOR CAPSULOTOMY MODEL 100 (P830062/S016) | Nidek, Inc. | 1990-03-13 |
| ND:YAG POSTERIOR CAPSULOTOMY MODEL 100 (P830062/S015) | Nidek, Inc. | 1989-09-08 |
| ND:YAG POSTERIOR CAPSULOTOMY MODEL 100 (P830062/S014) | Nidek, Inc. | 1989-08-30 |
| ND:YAG POSTERIOR CAPSULOTOMY MODEL 100 (P830062/S012) | Nidek, Inc. | 1988-07-28 |
| ND:YAG POSTERIOR CAPSULOTOMY MODEL 100 (P830062/S011) | Nidek, Inc. | 1987-06-11 |
| ND:YAG POSTERIOR CAPSULOTOMY MODEL 100 (P830062/S009) | Nidek, Inc. | 1987-04-08 |
| ND:YAG POSTERIOR CAPSULOTOMY MODEL 100 (P830062/S010) | Nidek, Inc. | 1986-12-01 |
| ND:YAG POSTERIOR CAPSULOTOMY MODEL 100 (P830062/S007) | Nidek, Inc. | 1985-11-26 |