RAPID AUTOMATIC PNEUMOPERITONEUM-I— 510(k) K900808

Name: FDA 510(k) clearance K900808
Creator: U.S. Food and Drug Administration
Published: 1990-09-19

Substantially Equivalent

Trek Medical Products, Inc.

FDA 510(k) clearance K900808 for RAPID AUTOMATIC PNEUMOPERITONEUM-I, Substantially Equivalent on 1990-09-19. Applicant: Trek Medical Products, Inc.. Device class: 2.

Clearance details

Applicant: Trek Medical Products, Inc.
Product code: Code HIF
Device class: Class 2
Regulation: 21 CFR 884.1730
Advisory panel: Obstetrics/Gynecology
Date received: 1990-02-21
Decision date: 1990-09-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Muckwonago, WI, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HIF

view all

K260209 — ENDOFLATOR+; Smart Smoke Evacuation2026-08-19
K252584 — Insufflator (wAlcor C50A, wAlcor C50B, wAlcor C50C, wAlcor C35A, wAlcor C35B, wAlcor C35C)2026-06-25
K252318 — Insufflator (OPTO-IFL1000)2026-04-16
K250388 — ENDOFLATOR +2025-09-22
K242772 — AirSurgN Insufflator (10030/AirSurgN)2025-04-11

More clearances from Trek Medical Products, Inc.

view all

K920937 — COMPUTERIZED PUPIL1992-10-02
K920944 — FTS-200 GAS SYSTEM1992-05-29
K902784 — FIBER OPTIC LIGHT SOURCE1990-09-12
K895813 — GLAUCOMA MECHANICAL TREPHINE1990-04-30
K882403 — OPHTHALMIC FLUID INJECTOR1988-09-09

Adverse events under product code HIF

product code HIF

Death: 19
Injury: 578
Malfunction: 5,639
Total: 6,236

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.