KARAYA GUM POWDER— 510(k) K770230

Substantially Equivalent

Atlantic Surgical

FDA 510(k) clearance K770230 for KARAYA GUM POWDER, Substantially Equivalent on 1977-02-28. Applicant: Atlantic Surgical. Device class: 1.

Clearance details

Applicant: Atlantic Surgical
Product code: Code EZR
Device class: Class 1
Regulation: 21 CFR 876.5900
Advisory panel: Gastroenterology, Urology
Date received: 1977-02-07
Decision date: 1977-02-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code EZR

K844341 — UNITED SKIN BARRIER PASTE1985-01-18
K803100 — STOMAHESIVE PASTE PROTECTIVE SKIN BARR1981-01-08
K791146 — COLO-TAPE1979-07-30
K761340 — OSTOMY KARAYA GUM POWDER1977-03-07
K761319 — KARAYA GUM PRODUCTS - PROCESS CHANGE1977-02-15

More clearances from Atlantic Surgical

K820167 — LAMINATED KARAYA GUM WASHERS1982-02-18
K772366 — BAG, DRAINAGEW/ADHESIVE; PROSTHESIS1978-01-26

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