K792306 is the FDA 510(k) clearance record for RH VIEWBOX, a class I device, cleared for Tekpro on 1979-12-04 under FDA product code KSY (Boxes, View, Blood Grouping). FDA records list 2 510(k) clearances for Tekpro, from 1979-01-03 to 1979-12-04 . As of 2026-09-10 , FDA records show no recalls naming K792306.
Clearance record Decision date 1979-12-04 Received 1979-11-16 (18 days to decision) Product code KSY Boxes, View, Blood GroupingRegulation 21 CFR 864.9185 Device class Class I Review panel Hematology Applicant Tekpro 803 N. Front St. Suite 3, Mchenry IL Third party review No
Clearances, product code KSY Trailing 12 months FDA records hold no clearances under product code KSY in the trailing twelve months.
FDA records show no clearances under product code KSY in the twelve months to October 2026. Show the numbers FIRST ARTICLE / WEEKLY
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Product code KSY
FDA records show no recalls under product code KSY.
MDM coverage of this record lists here, newest first.
About this record Sourced from the FDA 510(k) premarket notification database, ingested from openFDA. MDM adds the decision time in days, the product code cross-link, recalls sharing that product code, and MDM coverage of the record.
Predicate devices are not listed. The openFDA 510(k) endpoint does not publish predicate references, so MDM does not assert them. Where a 510(k) summary exists, the FDA PDF is linked above and names the predicate itself.
Data as of 2026-09-28 , the FDA export date for this dataset. Page last changed 2026-09-05 . View this record on fda.gov ↗ (opens on fda.gov)
