SCANNING SYS., AUTO. COMP., ACS1000

Device, Automated Cell-locating

HONEYWELL, INC.

The following data is part of a premarket notification filed by Honeywell, Inc. with the FDA for Scanning Sys., Auto. Comp., Acs1000.

Pre-market Notification Details

Device IDK772140
510k NumberK772140
Device Name:SCANNING SYS., AUTO. COMP., ACS1000
ClassificationDevice, Automated Cell-locating
Applicant HONEYWELL, INC. 803 N. Front St. Suite 3 Mchenry,  IL  60050
Product CodeJOY  
CFR Regulation Number864.5260 [🔎]
DecisionSubstantially Equivalent (SESE)
TypeTraditional
3rd Party ReviewedNo
Combination ProductNo
Date Received1977-11-14
Decision Date1977-12-05

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