PISTON SYRINGE— 510(k) K944941

Substantially Equivalent

Martell Medical Products, Inc.

FDA 510(k) clearance K944941 for PISTON SYRINGE, Substantially Equivalent on 1994-12-05. Applicant: Martell Medical Products, Inc.. Device class: 1.

Clearance details

Applicant: Martell Medical Products, Inc.
Product code: Code CBT
Device class: Class 1
Regulation: 21 CFR 868.1100
Advisory panel: Anesthesiology
Date received: 1994-10-07
Decision date: 1994-12-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Murrieta, CA, US

Download summary PDF View on FDA.gov ↗

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Recalls naming K944941

K-number listed on FDA's recall record

Z-1779-2022 — Full Kit Pulset 3cc Syringe 23g x 1 Safety Tip 25u BH, REF Number 3373-91Class II·Terminated·SunMed Holdings, LLC·20220908

Matched by K-number from FDA's Recall Enterprise System record (openFDA device/recallk_numbers) — these recalls explicitly list K944941.

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