LANCER ICE CUBE— 510(k) K782077

Substantially Equivalent

Sherwood Medical Industries

FDA 510(k) clearance K782077 for LANCER ICE CUBE, Substantially Equivalent on 1979-04-03. Applicant: Sherwood Medical Industries. Device class: 1.

Clearance details

Applicant: Sherwood Medical Industries
Product code: Code JRM
Device class: Class 1
Regulation: 21 CFR 862.2050
Advisory panel: Clinical Chemistry
Date received: 1978-12-13
Decision date: 1979-04-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code JRM

K921568 — ORS-1001992-06-09
K921569 — ORS-2001992-06-09
K921570 — ORS-3001992-06-09
K915427 — ORS-10001992-01-07
K913777 — SELF-CONTAINED SURGICAL SLUSH FREEZER1991-09-25

More clearances from Sherwood Medical Industries

K801070 — SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLES1980-07-21
K801071 — LANCER GLUCOSE RATE REAGENT KIT1980-05-23
K792013 — LANCER L-INA HUMAN REFERENCE SERUM1979-11-13
K792014 — LANCER L-INA BUFFER, POLYMER, WASH SOLU1979-11-13
K790523 — ARGYLE ESOPHAGEAL STETHOSCOPE1979-03-27

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