LEAD INTRODUCER SETS-EB-S8 & EB-S12
K-Number: K831751 · 1983-10-20
Advertisement
Device Summary
Frequently Asked Questions
What is the LEAD INTRODUCER SETS-EB-S8 & EB-S12?
LEAD INTRODUCER SETS-EB-S8 & EB-S12 is a medical device that received FDA 510(k) clearance on 1983-10-20. The listed applicant is Oscor, Inc.. The 510(k) number is K831751.
When did LEAD INTRODUCER SETS-EB-S8 & EB-S12 receive FDA 510(k) clearance?
LEAD INTRODUCER SETS-EB-S8 & EB-S12 received FDA 510(k) clearance on 1983-10-20, under 510(k) number K831751.
Who is the listed applicant for LEAD INTRODUCER SETS-EB-S8 & EB-S12?
The FDA 510(k) record lists Oscor, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LEAD INTRODUCER SETS-EB-S8 & EB-S12?
The FDA product code for LEAD INTRODUCER SETS-EB-S8 & EB-S12 is DYB.
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 Oscor, 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: DYB)
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.
Advertisement