510(k) K771714
- Device
- SLIDE STAINERS GLS 360 & 360-1
- Applicant
- Honeywell, Inc.
- 510(k) number
- K771714
- Product code
- KEY
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1977-10-05
- Date received
- 1977-09-12
- Regulation
- 864.3800
- Classification name
- Stainer, Tissue, Automated
- Medical specialty
- Pathology
- Review panel
- Pathology
- Device class
- 1
- Clearance type
- Traditional
- Third party reviewed
- N
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 3010685493
- 1063851
- 3010303097
- 3005248192
- 3002805583
- 3010781643
- 9613079
- 3004215117
- 2954792
- 1000391282
- 3008776165
- 3008399755
Source Documents#
510(k) summary PDF not indicated by FDA