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)

4 X 4 STERILE GAUZE SPONGE TRAY

K-Number: K893902 · 1989-07-14

Decision Date1989-07-14
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

4 X 4 STERILE GAUZE SPONGE TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Mumtaz I. Malik. It received FDA 510(k) clearance on 1989-07-14 under 510(k) number K893902. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 4 X 4 STERILE GAUZE SPONGE TRAY?

4 X 4 STERILE GAUZE SPONGE TRAY is a medical device that received FDA 510(k) clearance on 1989-07-14. The listed applicant is Mumtaz I. Malik. The 510(k) number is K893902.

When did 4 X 4 STERILE GAUZE SPONGE TRAY receive FDA 510(k) clearance?

4 X 4 STERILE GAUZE SPONGE TRAY received FDA 510(k) clearance on 1989-07-14, under 510(k) number K893902.

Who is the listed applicant for 4 X 4 STERILE GAUZE SPONGE TRAY?

The FDA 510(k) record lists Mumtaz I. Malik as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 4 X 4 STERILE GAUZE SPONGE TRAY?

The FDA product code for 4 X 4 STERILE GAUZE SPONGE TRAY is EFQ.

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 Mumtaz I. Malik 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 7 devices →

Related Devices (Code: EFQ)

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.

↑