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FDA 510(k)

VANISHPOINT SYRINGE

K-Number: K980069 · 1998-02-12

Decision Date1998-02-12
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VANISHPOINT SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Retractable Technologies, Inc.. It received FDA 510(k) clearance on 1998-02-12 under 510(k) number K980069. 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 VANISHPOINT SYRINGE?

VANISHPOINT SYRINGE is a medical device that received FDA 510(k) clearance on 1998-02-12. The listed applicant is Retractable Technologies, Inc.. The 510(k) number is K980069.

When did VANISHPOINT SYRINGE receive FDA 510(k) clearance?

VANISHPOINT SYRINGE received FDA 510(k) clearance on 1998-02-12, under 510(k) number K980069.

Who is the listed applicant for VANISHPOINT SYRINGE?

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

What is the FDA product code for VANISHPOINT SYRINGE?

The FDA product code for VANISHPOINT 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 Retractable Technologies, 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: 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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