TECHNICON AUTOSLIDE STAINING/PROCESSING— 510(k) K781598

Name: FDA 510(k) clearance K781598
Creator: U.S. Food and Drug Administration
Published: 1978-10-17

Substantially Equivalent

Technicon Instruments Corp.

FDA 510(k) clearance K781598 for TECHNICON AUTOSLIDE STAINING/PROCESSING, Substantially Equivalent on 1978-10-17. Applicant: Technicon Instruments Corp.. Device class: 1.

Clearance details

Applicant: Technicon Instruments Corp.
Product code: Code KPA
Device class: Class 1
Regulation: 21 CFR 864.3800
Advisory panel: Pathology
Date received: 1978-09-18
Decision date: 1978-10-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KPA

view all

K933996 — PROFIBLOT1994-01-28
K884258 — VERSABLOT1988-12-14
K881592 — WESCOR MODEL 7300 AEROSPRAY GRAM STAINER1988-05-13
K880745 — LX-100 SLIDE STAINER1988-04-27
K874887 — WESBLOT PROCESSOR1988-03-24

More clearances from Technicon Instruments Corp.

view all

K914511 — TECHNICON AXON(TM) SYSTEM METHODS ANYALYE HDL CHOL1991-11-27
K914888 — TECHNICON CHEM 1(TM) SYST (GEN2 SYST)1991-11-27
K914025 — TECHNICON AXON(TM) SYSTEMS, ALT(P 5-P)/AST(P 5-P)1991-11-22
K912616 — TECHNICON IMMUNO 1 TM SYSTEM ADDITIONAL ANALYTES1991-09-25
K912413 — CHEM-LINK DATA BASE MANAGER1991-07-01

Adverse events under product code KPA

product code KPA

Malfunction: 1,177
Total: 1,177

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.