UNIVEC AUTO-DISABLE HYPODERMIC SYRINGE
K-Number: K993996 · 2000-07-17
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Device Summary
Frequently Asked Questions
What is the UNIVEC AUTO-DISABLE HYPODERMIC SYRINGE?
UNIVEC AUTO-DISABLE HYPODERMIC SYRINGE is a medical device that received FDA 510(k) clearance on 2000-07-17. The listed applicant is Univec, Inc.. The 510(k) number is K993996.
When did UNIVEC AUTO-DISABLE HYPODERMIC SYRINGE receive FDA 510(k) clearance?
UNIVEC AUTO-DISABLE HYPODERMIC SYRINGE received FDA 510(k) clearance on 2000-07-17, under 510(k) number K993996.
Who is the listed applicant for UNIVEC AUTO-DISABLE HYPODERMIC SYRINGE?
The FDA 510(k) record lists Univec, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for UNIVEC AUTO-DISABLE HYPODERMIC SYRINGE?
The FDA product code for UNIVEC AUTO-DISABLE HYPODERMIC 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 Univec, 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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