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FDA 510(k)

DISPOSABLE SYRINGES AND DISPOSABLE NEEDLES

K-Number: K945225 · 1995-01-26

Decision Date1995-01-26
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE SYRINGES AND DISPOSABLE NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is Myco Medical Supplies, Inc.. It received FDA 510(k) clearance on 1995-01-26 under 510(k) number K945225. 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 SYRINGES AND DISPOSABLE NEEDLES?

DISPOSABLE SYRINGES AND DISPOSABLE NEEDLES is a medical device that received FDA 510(k) clearance on 1995-01-26. The listed applicant is Myco Medical Supplies, Inc.. The 510(k) number is K945225.

When did DISPOSABLE SYRINGES AND DISPOSABLE NEEDLES receive FDA 510(k) clearance?

DISPOSABLE SYRINGES AND DISPOSABLE NEEDLES received FDA 510(k) clearance on 1995-01-26, under 510(k) number K945225.

Who is the listed applicant for DISPOSABLE SYRINGES AND DISPOSABLE NEEDLES?

The FDA 510(k) record lists Myco Medical Supplies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE SYRINGES AND DISPOSABLE NEEDLES?

The FDA product code for DISPOSABLE SYRINGES AND DISPOSABLE NEEDLES 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.

Other records listing Myco Medical Supplies, Inc. as applicant

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.

View all 12 devices →

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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