NEEDLES, STERILE, AIRWAY
FDA 510(k) clearance K770425 · decided 1977-04-15
Clearance details
- K-number
- K770425
- Device name
- NEEDLES, STERILE, AIRWAY
- Applicant
- Pfizer Pharmaceuticals
- Decision
- Substantially Equivalent
- Date received
- 1977-03-07
- Decision date
- 1977-04-15
- Days to decision
- 39 days
- Clearance type
- Traditional
- Product code
- FMI
- Device class
- 2
- Regulation number
- 880.5570
- Medical specialty
- General Hospital
- Advisory committee
- General Hospital
- 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.