REMINGTON MEDICAL DISPOS TEAR-AWAY VASC INTRO SET
K-Number: K932370 · 1993-11-09
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Device Summary
Frequently Asked Questions
What is the REMINGTON MEDICAL DISPOS TEAR-AWAY VASC INTRO SET?
REMINGTON MEDICAL DISPOS TEAR-AWAY VASC INTRO SET is a medical device that received FDA 510(k) clearance on 1993-11-09. The listed applicant is Remington Medical, Inc.. The 510(k) number is K932370.
When did REMINGTON MEDICAL DISPOS TEAR-AWAY VASC INTRO SET receive FDA 510(k) clearance?
REMINGTON MEDICAL DISPOS TEAR-AWAY VASC INTRO SET received FDA 510(k) clearance on 1993-11-09, under 510(k) number K932370.
Who is the listed applicant for REMINGTON MEDICAL DISPOS TEAR-AWAY VASC INTRO SET?
The FDA 510(k) record lists Remington Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for REMINGTON MEDICAL DISPOS TEAR-AWAY VASC INTRO SET?
The FDA product code for REMINGTON MEDICAL DISPOS TEAR-AWAY VASC INTRO SET 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 Remington Medical, 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.
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