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)

DISPOSABLE RETRACTABLE NEEDLE SYRINGE

K-Number: K910731 · 1991-05-07

Decision Date1991-05-07
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE RETRACTABLE NEEDLE SYRINGE is the device name listed in this FDA 510(k) record. The listed applicant is Safe Tech Medical Products, Inc.. It received FDA 510(k) clearance on 1991-05-07 under 510(k) number K910731. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE RETRACTABLE NEEDLE SYRINGE?

DISPOSABLE RETRACTABLE NEEDLE SYRINGE is a medical device that received FDA 510(k) clearance on 1991-05-07. The listed applicant is Safe Tech Medical Products, Inc.. The 510(k) number is K910731.

When did DISPOSABLE RETRACTABLE NEEDLE SYRINGE receive FDA 510(k) clearance?

DISPOSABLE RETRACTABLE NEEDLE SYRINGE received FDA 510(k) clearance on 1991-05-07, under 510(k) number K910731.

Who is the listed applicant for DISPOSABLE RETRACTABLE NEEDLE SYRINGE?

The FDA 510(k) record lists Safe Tech Medical Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE RETRACTABLE NEEDLE SYRINGE?

The FDA product code for DISPOSABLE RETRACTABLE NEEDLE SYRINGE is FMF.

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 Safe Tech Medical Products, 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: FMF)

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.

↑