SR-MODEL 230 (MODIFICATION)— 510(k) K864106
Substantially EquivalentHirata Sangyo Co. USA, Inc.
FDA 510(k) clearance K864106 for SR-MODEL 230 (MODIFICATION), Substantially Equivalent on 1986-11-19. Applicant: Hirata Sangyo Co. USA, Inc.. Device class: 2.
Clearance details
- Applicant
- Hirata Sangyo Co. USA, Inc.
- Product code
- Code FRN
- Device class
- Class 2
- Regulation
- 21 CFR 880.5725
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Los Angeles, CA, US
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More clearances from Hirata Sangyo Co. USA, Inc.
view allAdverse events under product code FRN
product code FRN- Death
- 540
- Injury
- 6,178
- Malfunction
- 1,464,165
- Other
- 52
- Total
- 1,470,935
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.