ANSPACH LEG SUPPORT— 510(k) K801330
Substantially EquivalentThe Anspach Effort, Inc.
FDA 510(k) clearance K801330 for ANSPACH LEG SUPPORT, Substantially Equivalent on 1980-06-26. Applicant: The Anspach Effort, Inc.. Device class: 1.
Clearance details
- Applicant
- The Anspach Effort, Inc.
- Product code
- Code CCX
- Device class
- Class 1
- Regulation
- 21 CFR 868.6820
- Advisory panel
- Anesthesiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, US
Recent devices under product code CCX
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- K180063 — OCM-G1 Attachment
- K133604 — ANSPACH EG1 HIGH SPEED SYSTEM, G1 ATTACHMENTS
- K131053 — ANSPACH XMAX, EMAX2 AND EMAX2 PLUS SYSTEM WITH OTOLOGIC ATTACHMENT SYSTEM
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