MINRAD DRTS LIGHT SABER SYRINGE
K-Number: K981140 · 1998-06-25
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Device Summary
Frequently Asked Questions
What is the MINRAD DRTS LIGHT SABER SYRINGE?
MINRAD DRTS LIGHT SABER SYRINGE is a medical device that received FDA 510(k) clearance on 1998-06-25. The listed applicant is Minrad, Inc.. The 510(k) number is K981140.
When did MINRAD DRTS LIGHT SABER SYRINGE receive FDA 510(k) clearance?
MINRAD DRTS LIGHT SABER SYRINGE received FDA 510(k) clearance on 1998-06-25, under 510(k) number K981140.
Who is the listed applicant for MINRAD DRTS LIGHT SABER SYRINGE?
The FDA 510(k) record lists Minrad, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MINRAD DRTS LIGHT SABER SYRINGE?
The FDA product code for MINRAD DRTS LIGHT SABER SYRINGE is FMF.
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 Minrad, 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: FMF)
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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