AKRO-SIL FOLEY KIT 5CC— 510(k) K771651

Substantially Equivalent

Latex Ind., Inc.

FDA 510(k) clearance K771651 for AKRO-SIL FOLEY KIT 5CC, Substantially Equivalent on 1977-09-20. Applicant: Latex Ind., Inc.. Device class: 2.

Clearance details

Applicant: Latex Ind., Inc.
Product code: Code FCM
Device class: Class 2
Regulation: 21 CFR 876.5130
Advisory panel: Gastroenterology, Urology
Date received: 1977-08-29
Decision date: 1977-09-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Latex Ind., Inc.

K812058 — AKRON URINARY DRAINAGE BAT1981-07-31
K810281 — UROLOGICAL CATHETERS1981-02-25
K791674 — BLADDER RETENTION CATHETERIZATION TRAY1979-11-05
K781751 — CATHETER, AKRON FOLEY TEFLON1979-01-22
K781433 — AKRON MALE EXTERNAL CATHETER1978-11-03

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