LABELING FOR MYO/WIRE II STERNOTOMY SUTURES— 510(k) K932513

Name: FDA 510(k) clearance K932513
Creator: U.S. Food and Drug Administration
Published: 1994-01-07

Substantially Equivalent

Alto Development Corp.

FDA 510(k) clearance K932513 for LABELING FOR MYO/WIRE II STERNOTOMY SUTURES, Substantially Equivalent on 1994-01-07. Applicant: Alto Development Corp.. Device class: 2.

Clearance details

Applicant: Alto Development Corp.
Product code: Code GAO
Device class: Class 2
Regulation: 21 CFR 878.4495
Advisory panel: General, Plastic Surgery
Date received: 1993-05-25
Decision date: 1994-01-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Farmingdale, NJ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GAO

view all

K872532 — AUTO SUTURE STAINLESS STEEL SUTURES*1987-08-05
K863034 — SHARPOINT STAINLESS STEEL SUTURE1986-09-30
K802248 — DISARP ORIGINAL1980-09-26

More clearances from Alto Development Corp.

view all

K964621 — A & E MEDICAL ELECTROCAUTERY SUCTION TUBE WITH FINGER TIP ACTIVATOR BUTTON1996-12-20
K931537 — A&E MEDICAL ELECTROSURG ELECTRO W/NON-STICK COAT1993-09-07
K930528 — A&E MEDICAL ELECTROSURGICAL CONNECTING CORDS1993-05-17
K914193 — A&E MEDICAL CORP DISPOS SUCT COAG W/NON STICK COAT1992-10-05
K915300 — A & EM MEDICAL ELECTROSURGICAL PENCIL/ACCESSORIES1992-02-18

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