INAMED DEVELOPMENT ASPIRATION TIP— 510(k) K931548

Name: FDA 510(k) clearance K931548
Creator: U.S. Food and Drug Administration
Published: 1994-01-10

Substantially Equivalent

Inamed Development Co.

FDA 510(k) clearance K931548 for INAMED DEVELOPMENT ASPIRATION TIP, Substantially Equivalent on 1994-01-10. Applicant: Inamed Development Co.. Device class: 2.

Clearance details

Applicant: Inamed Development Co.
Product code: Code GCX
Device class: Class 2
Regulation: 21 CFR 880.6740
Advisory panel: General Hospital
Date received: 1993-03-29
Decision date: 1994-01-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Carpinteria, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GCX

view all

K042454 — STRYKER CASSETTE PUMP2004-12-09
K992126 — CIRCON SURGIFLEX WAVE TSUNAMI SUCTION-IRRIGATION SYSTEM1999-08-03
K972074 — SUCTION INSTRUMENTATION1997-07-25
K971022 — CHASE SUCKER1997-04-17
K964127 — MEDI-VAC FLEXI-CLEAR SUCTION HANDLE1996-12-31

More clearances from Inamed Development Co.

view all

K904265 — INAMED RUIZ-COHEN INTRAOPERATIVE TISSUE EXPANDER1991-03-06
K901742 — INAMED SMALL DRAIN SYSTEM1990-05-07
K901764 — INAMED CONVERTIBLE DRAIN SYSTEM1990-05-07
K894618 — INAMED RHEMO-D (TM) DILATOR1990-01-18
K896491 — INAMED CLOSED-WOUND DRAIN SYSTEM1990-01-08

Adverse events under product code GCX

product code GCX

Death: 9
Malfunction: 592
Other: 2
Total: 603

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.