BOSTON SYRINGE
K-Number: K820294 · 1982-03-23
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Device Summary
Frequently Asked Questions
What is the BOSTON SYRINGE?
BOSTON SYRINGE is a medical device that received FDA 510(k) clearance on 1982-03-23. The listed applicant is Frisco Products, Inc.. The 510(k) number is K820294.
When did BOSTON SYRINGE receive FDA 510(k) clearance?
BOSTON SYRINGE received FDA 510(k) clearance on 1982-03-23, under 510(k) number K820294.
Who is the listed applicant for BOSTON SYRINGE?
The FDA 510(k) record lists Frisco Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BOSTON SYRINGE?
The FDA product code for BOSTON 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 Frisco Products, 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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