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FDA 510(k)

REUSABLE ALL - GLASS SYRINGES

K-Number: K944542 · 1995-09-29

Decision Date1995-09-29
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

REUSABLE ALL - GLASS SYRINGES is the device name listed in this FDA 510(k) record. The listed applicant is Top Syringe Mfg. Co.. It received FDA 510(k) clearance on 1995-09-29 under 510(k) number K944542. 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 REUSABLE ALL - GLASS SYRINGES?

REUSABLE ALL - GLASS SYRINGES is a medical device that received FDA 510(k) clearance on 1995-09-29. The listed applicant is Top Syringe Mfg. Co.. The 510(k) number is K944542.

When did REUSABLE ALL - GLASS SYRINGES receive FDA 510(k) clearance?

REUSABLE ALL - GLASS SYRINGES received FDA 510(k) clearance on 1995-09-29, under 510(k) number K944542.

Who is the listed applicant for REUSABLE ALL - GLASS SYRINGES?

The FDA 510(k) record lists Top Syringe Mfg. Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for REUSABLE ALL - GLASS SYRINGES?

The FDA product code for REUSABLE ALL - GLASS SYRINGES 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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