30-30-2 700 SYRINGE EXTENSION SET
K-Number: K811885 · 1981-08-25
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Device Summary
Frequently Asked Questions
What is the 30-30-2 700 SYRINGE EXTENSION SET?
30-30-2 700 SYRINGE EXTENSION SET is a medical device that received FDA 510(k) clearance on 1981-08-25. The listed applicant is Y. The 510(k) number is K811885.
When did 30-30-2 700 SYRINGE EXTENSION SET receive FDA 510(k) clearance?
30-30-2 700 SYRINGE EXTENSION SET received FDA 510(k) clearance on 1981-08-25, under 510(k) number K811885.
Who is the listed applicant for 30-30-2 700 SYRINGE EXTENSION SET?
The FDA 510(k) record lists Y as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 30-30-2 700 SYRINGE EXTENSION SET?
The FDA product code for 30-30-2 700 SYRINGE EXTENSION SET is FPA.
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 Y 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: FPA)
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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