SYRINGE,PISTON NEEDLE, HOLLOW LUMEN
K-Number: K833460 · 1983-11-28
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Device Summary
Frequently Asked Questions
What is the SYRINGE,PISTON NEEDLE, HOLLOW LUMEN?
SYRINGE,PISTON NEEDLE, HOLLOW LUMEN is a medical device that received FDA 510(k) clearance on 1983-11-28. The listed applicant is Aldrich Chemical Co., Inc.. The 510(k) number is K833460.
When did SYRINGE,PISTON NEEDLE, HOLLOW LUMEN receive FDA 510(k) clearance?
SYRINGE,PISTON NEEDLE, HOLLOW LUMEN received FDA 510(k) clearance on 1983-11-28, under 510(k) number K833460.
Who is the listed applicant for SYRINGE,PISTON NEEDLE, HOLLOW LUMEN?
The FDA 510(k) record lists Aldrich Chemical Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SYRINGE,PISTON NEEDLE, HOLLOW LUMEN?
The FDA product code for SYRINGE,PISTON NEEDLE, HOLLOW LUMEN 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 Aldrich Chemical Co., 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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