LITHOTRITE
FDA 510(k) clearance K760273 · decided 1976-12-06
Clearance details
- K-number
- K760273
- Device name
- LITHOTRITE
- Applicant
- V. Mueller O.V. Baxter Healthcare Corp.
- Decision
- Substantially Equivalent
- Date received
- 1976-07-22
- Decision date
- 1976-12-06
- Days to decision
- 137 days
- Clearance type
- Traditional
- Product code
- FGK
- Device class
- 2
- Regulation number
- 876.4500
- Medical specialty
- Gastroenterology, Urology
- Advisory committee
- Gastroenterology, Urology
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.