Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

REMINGTON MEDICAL DISPOS TEAR-AWAY VASC INTRO SET

K-Number: K932370 · 1993-11-09

Decision Date1993-11-09
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

REMINGTON MEDICAL DISPOS TEAR-AWAY VASC INTRO SET is the device name listed in this FDA 510(k) record. The listed applicant is Remington Medical, Inc.. It received FDA 510(k) clearance on 1993-11-09 under 510(k) number K932370. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 18 devices →

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.

↑