ORTHOPEDIC TUBULAR STOCKINETTE— 510(k) K760817

Substantially Equivalent

Parke-Davis Co.

FDA 510(k) clearance K760817 for ORTHOPEDIC TUBULAR STOCKINETTE, Substantially Equivalent on 1976-10-20. Applicant: Parke-Davis Co.. Device class: 1.

Clearance details

Applicant: Parke-Davis Co.
Product code: Code ILG
Device class: Class 1
Regulation: 21 CFR 890.3475
Advisory panel: Physical Medicine
Date received: 1976-10-12
Decision date: 1976-10-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code ILG

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K780612 — STOCKINETTE, STERILE1978-04-19
K780547 — STERILE ORTHOPEDIC STOCKINETTE1978-04-10
K770346 — ORTHOPEDIC STOCKINETTE1977-03-07

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K860570 — ANGIO-FLO CONTINUOUS ARTERIAL CATH FLUSH DEVICE1986-03-31
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Data sourced from openFDA. This site is unofficial and independent of the FDA.