ARGYLE PEOCUSSOR SYSTEM
FDA 510(k) clearance K771876 · decided 1977-10-28
Clearance details
- K-number
- K771876
- Device name
- ARGYLE PEOCUSSOR SYSTEM
- Applicant
- Sherwood Medical Industries
- Decision
- Substantially Equivalent
- Date received
- 1977-10-04
- Decision date
- 1977-10-28
- Days to decision
- 24 days
- Clearance type
- Traditional
- Product code
- BYI
- Device class
- 2
- Regulation number
- 868.5665
- Medical specialty
- Anesthesiology
- Advisory committee
- Anesthesiology
- 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.