DAMON D.E.T.E.C.T IMAGE ENHANCER— 510(k) K874865

Name: FDA 510(k) clearance K874865
Creator: U.S. Food and Drug Administration
Published: 1987-12-23

Substantially Equivalent

Damon Corp.

FDA 510(k) clearance K874865 for DAMON D.E.T.E.C.T IMAGE ENHANCER, Substantially Equivalent on 1987-12-23. Applicant: Damon Corp.. Device class: 2.

Clearance details

Applicant: Damon Corp.
Product code: Code LLZ
Device class: Class 2
Regulation: 21 CFR 892.2050
Advisory panel: Radiology
Date received: 1987-11-27
Decision date: 1987-12-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: North Attleboro, MA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LLZ

view all

More clearances from Damon Corp.

view all

K831826 — ADRENOCORTICOTROPIN RADIO-IMMUNOASSAY1983-07-18
K820686 — LIQUISOL PROGESTERONE RADIOIMMUNO1982-04-01
K802661 — LIQUISOL TESTOSTERONE RADIOIMM. TEST KIT1980-12-10
K790250 — LIQUISOL CORTISOL RIA TEST KIT1979-04-04
K782124 — IEC CENTRA-7 CENTRIFUGE MODEL 23621979-02-26

Adverse events under product code LLZ

product code LLZ

Death: 13
Total: 13

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.