MICROLET FAMILY OF NEEDLE/DEPTH ELECT-— 510(k) K802249

Name: FDA 510(k) clearance K802249
Creator: U.S. Food and Drug Administration
Published: 1980-11-19

Substantially Equivalent

Progress Mankind Technology

FDA 510(k) clearance K802249 for MICROLET FAMILY OF NEEDLE/DEPTH ELECT-, Substantially Equivalent on 1980-11-19. Applicant: Progress Mankind Technology. Device class: 2.

Clearance details

Applicant: Progress Mankind Technology
Product code: Code GZL
Device class: Class 2
Regulation: 21 CFR 882.1330
Advisory panel: Neurology
Date received: 1980-09-16
Decision date: 1980-11-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hopkins, MN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GZL

view all

K253970 — Wovyn Depth Electrode2026-04-17
K250363 — Depth Electrode (17+ models)2025-11-05
K250601 — Neuro Omega System; NeuroSmart System2025-03-30
K223269 — Spencer Probe Depth Electrodes2023-05-18
K223276 — Anchor Bolts as Accessories to Depth Electrodes2023-05-18

More clearances from Progress Mankind Technology

view all

K883314 — PMT 3721-1 EPIDURAL KIT1988-10-28
K881616 — PMT MANKIND LUMBAR-PERITONEAL SHUNT MODEL 1115-11988-09-09
K871663 — PMT TRACTION TONGS1987-06-19
K854157 — PMT ACCUPRESSURE INFUSION SYSTEM 36011986-02-13
K845035 — ELECTRODE FOR NEUROLOGICAL SURGERY 21111985-07-30

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