POREX QUALITY PLASTIC SURGERY INSTRUMENTS— 510(k) K872947

Name: FDA 510(k) clearance K872947
Creator: U.S. Food and Drug Administration
Published: 1987-08-21

Substantially Equivalent

Porex Medical

FDA 510(k) clearance K872947 for POREX QUALITY PLASTIC SURGERY INSTRUMENTS, Substantially Equivalent on 1987-08-21. Applicant: Porex Medical. Device class: 1.

Clearance details

Applicant: Porex Medical
Product code: Code KDG
Device class: Class 1
Regulation: 21 CFR 878.4820
Advisory panel: General, Plastic Surgery
Date received: 1987-07-28
Decision date: 1987-08-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fairburn, GA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KDG

view all

K952678 — STA-CLEAR ALCOHOL-FREE ENDOSCOPIC ANTI-FOG KIT1995-07-10
K952200 — OMNI-JUG1995-06-29
K894785 — SURGICAL CHISEL/OSTEOTOME1989-08-18
K891471 — SIL-MED WASTE FLUID DUMP BAG1989-08-15
K872092 — OSTEOTOME SET, HOKE, STRAIGHT, SET OF 51987-06-23

More clearances from Porex Medical

view all

K872791 — POREX NERVE LOCATOR1987-10-20
K873044 — POREX OTOLOGY INSTRUMENTS1987-09-04
K863943 — POREX(TM) EYE SPHERE IMPLANT1987-02-27
K863946 — POREX(TM) EXTRA-OCULAR ORBITAL IMPLANT1987-02-27
K870154 — POREX(TM) TISSUE EXPANDER1987-02-24

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