AUTO. SLIDE STAINER— 510(k) K780017

Name: FDA 510(k) clearance K780017
Creator: U.S. Food and Drug Administration
Published: 1978-01-30

Substantially Equivalent

Honeywell, Inc.

FDA 510(k) clearance K780017 for AUTO. SLIDE STAINER, Substantially Equivalent on 1978-01-30. Applicant: Honeywell, Inc.. Device class: 1.

Clearance details

Applicant: Honeywell, Inc.
Product code: Code KPA
Device class: Class 1
Regulation: 21 CFR 864.3800
Advisory panel: Pathology
Date received: 1978-01-03
Decision date: 1978-01-30
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 Honeywell, Inc.

view all

K902230 — COLORADO COLOR IMAGING RECORDER1990-06-19
K863100 — CEN STA MON AC/DC ALARM CENTRAL ACCES ALARM RECOR1987-02-03
K853501 — HONEYWELL ELECTRONIC VENTILATOR EV-A1986-04-04
K855125 — PHYSIOLOGICAL TELEMETRY PATIENT MONITORING SYSTEM1986-03-26
K851888 — APM DISPOS. BLOOD PRESSURE TRANSDUCER1985-08-06

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.