DISPOSABLE PLASTIC SYRINGE & NEEDLE
K-Number: K820062 · 1982-04-01
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Device Summary
Frequently Asked Questions
What is the DISPOSABLE PLASTIC SYRINGE & NEEDLE?
DISPOSABLE PLASTIC SYRINGE & NEEDLE is a medical device that received FDA 510(k) clearance on 1982-04-01. The listed applicant is Marshall Davis, Inc.. The 510(k) number is K820062.
When did DISPOSABLE PLASTIC SYRINGE & NEEDLE receive FDA 510(k) clearance?
DISPOSABLE PLASTIC SYRINGE & NEEDLE received FDA 510(k) clearance on 1982-04-01, under 510(k) number K820062.
Who is the listed applicant for DISPOSABLE PLASTIC SYRINGE & NEEDLE?
The FDA 510(k) record lists Marshall Davis, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DISPOSABLE PLASTIC SYRINGE & NEEDLE?
The FDA product code for DISPOSABLE PLASTIC SYRINGE & NEEDLE is FMF.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: FMF)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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