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FDA 510(k)

SQUARE ONE SAFETY SYRINGE

K-Number: K955030 · 1995-12-15

Decision Date1995-12-15
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SQUARE ONE SAFETY SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Square One Medical, LP. It received FDA 510(k) clearance on 1995-12-15 under 510(k) number K955030. 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 SQUARE ONE SAFETY SYRINGE?

SQUARE ONE SAFETY SYRINGE is a medical device that received FDA 510(k) clearance on 1995-12-15. The listed applicant is Square One Medical, LP. The 510(k) number is K955030.

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

SQUARE ONE SAFETY SYRINGE received FDA 510(k) clearance on 1995-12-15, under 510(k) number K955030.

Who is the listed applicant for SQUARE ONE SAFETY SYRINGE?

The FDA 510(k) record lists Square One Medical, LP as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SQUARE ONE SAFETY SYRINGE?

The FDA product code for SQUARE ONE 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.

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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