ULTIMATE SEAL— 510(k) K960401
Substantially EquivalentHans Rudolph, Inc.
FDA 510(k) clearance K960401 for ULTIMATE SEAL, Substantially Equivalent on 1996-06-20. Applicant: Hans Rudolph, Inc.. Device class: 1.
Clearance details
- Applicant
- Hans Rudolph, Inc.
- Product code
- Code KGB
- Device class
- Class 1
- Regulation
- 21 CFR 868.5570
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Kansas City, MO, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.