SNOWDEN-PENCER INSUFFLATOR TUBING SET— 510(k) K913835

Name: FDA 510(k) clearance K913835
Creator: U.S. Food and Drug Administration
Published: 1991-11-07

Substantially Equivalent

Snowden-Pencer

FDA 510(k) clearance K913835 for SNOWDEN-PENCER INSUFFLATOR TUBING SET, Substantially Equivalent on 1991-11-07. Applicant: Snowden-Pencer. Device class: 2.

Clearance details

Applicant: Snowden-Pencer
Product code: Code HIF
Device class: Class 2
Regulation: 21 CFR 884.1730
Advisory panel: Obstetrics/Gynecology
Date received: 1991-08-26
Decision date: 1991-11-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tucker, GA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HIF

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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

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K960400 — DIAMOND-TOUCH AND MICRO DIAMOND-TOUCH INSTRUMENTS/DIAMOND-LINE INSTRUMENTS/DIAMOND-PORT(ACCESS PARTS)1996-03-12
K930666 — REUSABLE LAPAROSCOPIC INSTRUMENTS W/ ELECTROCAUTERY1994-05-19
K930667 — REUSABLE LAPAROSCOPIC INSTRUMENTS1994-05-16
K924148 — DIAMOND-SHARP(R) TROCARS1994-02-28
K924149 — ENDO I/A PROBE1993-01-26

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.