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FDA 510(k)

DISPOSABLE PLASTIC SYRINGE & NEEDLE

K-Number: K820062 · 1982-04-01

Decision Date1982-04-01
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE PLASTIC SYRINGE & NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Marshall Davis, Inc.. It received FDA 510(k) clearance on 1982-04-01 under 510(k) number K820062. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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