BAL CATH— 510(k) K923487

Unknown

Ballard Medical Products

FDA 510(k) clearance K923487 for BAL CATH, Unknown on 1993-07-30. Applicant: Ballard Medical Products. Device class: 2.

Clearance details

Applicant: Ballard Medical Products
Product code: Code KTR
Device class: Class 2
Regulation: 21 CFR 874.4680
Advisory panel: Ear, Nose, Throat
Date received: 1992-07-15
Decision date: 1993-07-30
Decision: Unknown
Clearance type: Traditional
Location: Draper, UT, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code KTR

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K820572 — ARGYLE DELEE SUCTION CATHETER W/MUCOUS1982-04-09
K791327 — ARGYLE TAUSSIG CULTURE CATHETER1979-08-22

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K000495 — BALLARD MEDICAL PRODUCTS EPIDURAL AND SPINAL NEEDLES2000-03-28
K993138 — BALLARD MIC-KEY G LOW PROFILE GASTROSTOMY REPLACEMENT KIT1999-10-20

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