AESCULAP THORACOSCOPIC INSTRUMENTS
FDA 510(k) clearance K944955 · decided 1994-11-09
Clearance details
- K-number
- K944955
- Device name
- AESCULAP THORACOSCOPIC INSTRUMENTS
- Applicant
- Aesculap, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1994-10-07
- Decision date
- 1994-11-09
- Days to decision
- 33 days
- Clearance type
- Traditional
- Product code
- KNS
- Device class
- 2
- Regulation number
- 876.4300
- Medical specialty
- Gastroenterology, Urology
- Advisory committee
- Gastroenterology, Urology
- Location
- South San Francisco, CA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
No recalls on record reference this clearance.