SUCTION RETRACTOR— 510(k) K875289

Name: FDA 510(k) clearance K875289
Creator: U.S. Food and Drug Administration
Published: 1988-01-22

Substantially Equivalent

T. Korossurgical Instruments Corp.

FDA 510(k) clearance K875289 for SUCTION RETRACTOR, Substantially Equivalent on 1988-01-22. Applicant: T. Korossurgical Instruments Corp.. Device class: 1.

Clearance details

Applicant: T. Korossurgical Instruments Corp.
Product code: Code GAD
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1987-12-30
Decision date: 1988-01-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Moorepark, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GAD

view all

K152538 — JRP Wound Spreader2016-04-13
K151104 — OTELO LL2016-01-06
K132645 — THORATRAK MICS RETRACTOR SYSTEM, RACK, BLADES2013-10-04
K071775 — DASH2007-08-07
K050256 — APPLE MEDICAL/OB MOBIUS ELASTIC RETRACTOR2005-04-26

More clearances from T. Korossurgical Instruments Corp.

view all

K001915 — GRAFT MARKER RING2001-04-27
K002755 — NON-ABSORBING STERNATOMY MONOFILAMENT SUTURE2000-12-04
K954016 — VIDEOSCOPE W/IRRIGATION SHEATH1996-01-25
K953998 — DISCETOME TISSUE ASPIRATOR1995-12-04
K954014 — PERCUTANEOUS DISCECTOMY CANNULA SYSTEM1995-11-06

Adverse events under product code GAD

product code GAD

Malfunction: 504
Total: 504

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.