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FDA 510(k)

SUPERGUARD SAFETY SYRINGE

K-Number: K990831 · 2000-03-08

Decision Date2000-03-08
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SUPERGUARD SAFETY SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is U.S. Safety Syringes Co., Inc.. It received FDA 510(k) clearance on 2000-03-08 under 510(k) number K990831. The device is classified under product code MEG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUPERGUARD SAFETY SYRINGE?

SUPERGUARD SAFETY SYRINGE is a medical device that received FDA 510(k) clearance on 2000-03-08. The listed applicant is U.S. Safety Syringes Co., Inc.. The 510(k) number is K990831.

When did SUPERGUARD SAFETY SYRINGE receive FDA 510(k) clearance?

SUPERGUARD SAFETY SYRINGE received FDA 510(k) clearance on 2000-03-08, under 510(k) number K990831.

Who is the listed applicant for SUPERGUARD SAFETY SYRINGE?

The FDA 510(k) record lists U.S. Safety Syringes Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUPERGUARD SAFETY SYRINGE?

The FDA product code for SUPERGUARD SAFETY SYRINGE is MEG.

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 U.S. Safety Syringes Co., 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 7 devices →

Related Devices (Code: MEG)

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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