SURGIN KIT
FDA 510(k) clearance K980849 · decided 1998-07-09
Clearance details
- K-number
- K980849
- Device name
- SURGIN KIT
- Applicant
- Surgin Surgical Instrumentation, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1998-02-05
- Decision date
- 1998-07-09
- Days to decision
- 154 days
- Clearance type
- Traditional
- Product code
- MSR
- Device class
- 2
- Regulation number
- 886.4150
- Medical specialty
- Ophthalmic
- Advisory committee
- Ophthalmic
- Location
- Tustin, CA, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Surgin Surgical Instrumentation
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 |
|---|---|---|
| TUBING EXTENSION SET (K993361) | Hurricane Medical | 2000-01-04 |
| ML UNIVERSAL TUBING (K983448) | Med-Logics, Inc. | 1998-12-18 |
| STORZ DP4210 VENTURI ECONOMY ANTERIOR PACK AND DP5000 ASC DAYPACK (K980100) | Storz Instrument Co. | 1998-06-01 |
| ML-DISPOSABLE PAK (K972522) | Med-Logics, Inc. | 1997-09-30 |
Recalls involving this device
No recalls on record reference this clearance.