ENDOSCOPIC INJECTION NEEDLE
K-Number: K820973 · 1982-04-16
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Device Summary
Frequently Asked Questions
What is the ENDOSCOPIC INJECTION NEEDLE?
ENDOSCOPIC INJECTION NEEDLE is a medical device that received FDA 510(k) clearance on 1982-04-16. The listed applicant is Mill-Rose Laboratory. The 510(k) number is K820973.
When did ENDOSCOPIC INJECTION NEEDLE receive FDA 510(k) clearance?
ENDOSCOPIC INJECTION NEEDLE received FDA 510(k) clearance on 1982-04-16, under 510(k) number K820973.
Who is the listed applicant for ENDOSCOPIC INJECTION NEEDLE?
The FDA 510(k) record lists Mill-Rose Laboratory as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENDOSCOPIC INJECTION NEEDLE?
The FDA product code for ENDOSCOPIC INJECTION NEEDLE is FBK.
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 Mill-Rose Laboratory 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: FBK)
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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