SLIDE STAINERS GLS 360 & 360-1
FDA 510(k) clearance K771714 · decided 1977-10-05
Clearance details
- K-number
- K771714
- Device name
- SLIDE STAINERS GLS 360 & 360-1
- Applicant
- Honeywell, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1977-09-12
- Decision date
- 1977-10-05
- Days to decision
- 23 days
- Clearance type
- Traditional
- Product code
- KEY
- Device class
- 1
- Regulation number
- 864.3800
- Medical specialty
- Pathology
- Advisory committee
- Pathology
- 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.