VANISHPOINT SYRINGE
K-Number: K980069 · 1998-02-12
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Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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