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)

RADIATION STERILIZATION OF SURG. GLOVES

K-Number: K823234 · 1984-04-17

Decision Date1984-04-17
Product Code
DecisionSubstantially Equivalent

Device Summary

RADIATION STERILIZATION OF SURG. GLOVES is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1984-04-17 under 510(k) number K823234. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RADIATION STERILIZATION OF SURG. GLOVES?

RADIATION STERILIZATION OF SURG. GLOVES is a medical device that received FDA 510(k) clearance on 1984-04-17. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K823234.

When did RADIATION STERILIZATION OF SURG. GLOVES receive FDA 510(k) clearance?

RADIATION STERILIZATION OF SURG. GLOVES received FDA 510(k) clearance on 1984-04-17, under 510(k) number K823234.

Who is the listed applicant for RADIATION STERILIZATION OF SURG. GLOVES?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

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 Bd Becton Dickinson Vacutainer Systems Preanalytic 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 632 devices →

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.

↑