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)

LORREX POST OPERATIVE SPONGES

K-Number: K942691 · 1994-07-19

Decision Date1994-07-19
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

LORREX POST OPERATIVE SPONGES is the device name listed in this FDA 510(k) record. The listed applicant is Lorons International Corp.. It received FDA 510(k) clearance on 1994-07-19 under 510(k) number K942691. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LORREX POST OPERATIVE SPONGES?

LORREX POST OPERATIVE SPONGES is a medical device that received FDA 510(k) clearance on 1994-07-19. The listed applicant is Lorons International Corp.. The 510(k) number is K942691.

When did LORREX POST OPERATIVE SPONGES receive FDA 510(k) clearance?

LORREX POST OPERATIVE SPONGES received FDA 510(k) clearance on 1994-07-19, under 510(k) number K942691.

Who is the listed applicant for LORREX POST OPERATIVE SPONGES?

The FDA 510(k) record lists Lorons International Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LORREX POST OPERATIVE SPONGES?

The FDA product code for LORREX POST OPERATIVE SPONGES 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 Lorons International Corp. 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: 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.

↑