KARL STORZ MODEL 203020 20 EQUIMAT— 510(k) K971982
Substantially EquivalentKARL STORZ Endoscopy-America, Inc.
FDA 510(k) clearance K971982 for KARL STORZ MODEL 203020 20 EQUIMAT, Substantially Equivalent on 1997-08-12. Applicant: KARL STORZ Endoscopy-America, Inc.. Device class: 2.
Clearance details
- Applicant
- KARL STORZ Endoscopy-America, Inc.
- Product code
- Code LJH
- Device class
- Class 2
- Regulation
- 21 CFR 876.5130
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Culver City, CA, US
Recent devices under product code LJH
view allMore clearances from KARL STORZ Endoscopy-America, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.