DeviceClearance

JARIT HULKA UTERINE TENACULUM FORCEPS— 510(k) K082349

Substantially Equivalent

J. Jamner Surgical Instruments, Inc.

FDA 510(k) clearance K082349 for JARIT HULKA UTERINE TENACULUM FORCEPS, Substantially Equivalent on 2008-11-21. Applicant: J. Jamner Surgical Instruments, Inc.. Device class: 2.

Clearance details

Applicant
J. Jamner Surgical Instruments, Inc.
Product code
Code HDC
Device class
Class 2
Regulation
21 CFR 884.4530
Advisory panel
Obstetrics/Gynecology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
York, PA, US
Download summary PDFView on FDA.gov ↗

Recent devices under product code HDC

view all

More clearances from J. Jamner Surgical Instruments, Inc.

view all

Recalls naming K082349

K-number listed on FDA's recall record

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K082349.

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