ALLISON MEDICAL SYRINGE
K-Number: K932001 · 1994-01-21
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Device Summary
Frequently Asked Questions
What is the ALLISON MEDICAL SYRINGE?
ALLISON MEDICAL SYRINGE is a medical device that received FDA 510(k) clearance on 1994-01-21. The listed applicant is Allison Medical, Inc.. The 510(k) number is K932001.
When did ALLISON MEDICAL SYRINGE receive FDA 510(k) clearance?
ALLISON MEDICAL SYRINGE received FDA 510(k) clearance on 1994-01-21, under 510(k) number K932001.
Who is the listed applicant for ALLISON MEDICAL SYRINGE?
The FDA 510(k) record lists Allison Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ALLISON MEDICAL SYRINGE?
The FDA product code for ALLISON MEDICAL 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 Allison Medical, 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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