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)

INSOSAFE BAK'SNAP RETRACTABLE INSULIN SAFETY SYRINGE

K-Number: K050131 · 2005-04-05

Decision Date2005-04-05
Product CodeMEG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INSOSAFE BAK'SNAP RETRACTABLE INSULIN SAFETY SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is M.K. Meditech Co. , Ltd.. It received FDA 510(k) clearance on 2005-04-05 under 510(k) number K050131. The device is classified under product code MEG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSOSAFE BAK'SNAP RETRACTABLE INSULIN SAFETY SYRINGE?

INSOSAFE BAK'SNAP RETRACTABLE INSULIN SAFETY SYRINGE is a medical device that received FDA 510(k) clearance on 2005-04-05. The listed applicant is M.K. Meditech Co. , Ltd.. The 510(k) number is K050131.

When did INSOSAFE BAK'SNAP RETRACTABLE INSULIN SAFETY SYRINGE receive FDA 510(k) clearance?

INSOSAFE BAK'SNAP RETRACTABLE INSULIN SAFETY SYRINGE received FDA 510(k) clearance on 2005-04-05, under 510(k) number K050131.

Who is the listed applicant for INSOSAFE BAK'SNAP RETRACTABLE INSULIN SAFETY SYRINGE?

The FDA 510(k) record lists M.K. Meditech Co. , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INSOSAFE BAK'SNAP RETRACTABLE INSULIN SAFETY SYRINGE?

The FDA product code for INSOSAFE BAK'SNAP RETRACTABLE INSULIN SAFETY SYRINGE is MEG.

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 M.K. Meditech Co. , Ltd. 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: MEG)

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.

↑