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FDA 510(k)

EASYSAFE RETRACTING NEEDLE SYRINGE

K-Number: K991039 · 1999-05-21

Decision Date1999-05-21
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

EASYSAFE RETRACTING NEEDLE SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Saf-T-Med, Inc.. It received FDA 510(k) clearance on 1999-05-21 under 510(k) number K991039. 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 EASYSAFE RETRACTING NEEDLE SYRINGE?

EASYSAFE RETRACTING NEEDLE SYRINGE is a medical device that received FDA 510(k) clearance on 1999-05-21. The listed applicant is Saf-T-Med, Inc.. The 510(k) number is K991039.

When did EASYSAFE RETRACTING NEEDLE SYRINGE receive FDA 510(k) clearance?

EASYSAFE RETRACTING NEEDLE SYRINGE received FDA 510(k) clearance on 1999-05-21, under 510(k) number K991039.

Who is the listed applicant for EASYSAFE RETRACTING NEEDLE SYRINGE?

The FDA 510(k) record lists Saf-T-Med, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EASYSAFE RETRACTING NEEDLE SYRINGE?

The FDA product code for EASYSAFE RETRACTING NEEDLE SYRINGE 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 Saf-T-Med, 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.

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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