TOBRAMYCIN 125I RIA KIT— 510(k) K780182

Substantially Equivalent

New England Nuclear

FDA 510(k) clearance K780182 for TOBRAMYCIN 125I RIA KIT, Substantially Equivalent on 1978-02-13. Applicant: New England Nuclear. Device class: 2.

Clearance details

Applicant: New England Nuclear
Product code: Code DID
Device class: Class 2
Regulation: 21 CFR 862.3900
Advisory panel: Clinical Toxicology
Date received: 1978-02-03
Decision date: 1978-02-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code DID

K820773 — EMIT-ST URINE COCAINE METABOLITE ASSAY1982-04-08
K802038 — PHENYTOIN REAGENT TEST KIT1980-10-23
K780950 — BIO-MONITOR TOBRAMYCIN1978-08-14
K780048 — AMINOGLYCOSIDE TEST SYSTEM1978-01-20

More clearances from New England Nuclear

K841478 — RIANEN CYCLIC-AMP RADIOIMMUNOASSAY1984-06-14
K840301 — RIANEN ESTRIOL RADIOIMMUNOASSAY KIT1984-03-30
K834038 — RIANEN FOLLICLE STIMULATING HORMONE1984-01-30
K833376 — RIANEN LUTEINIZING HORMONE RIA KIT1983-12-20
K831345 — RIANEN PROLACTIN 125I KIT1983-06-08

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