LORREX GAUZE SPONGES SPECIALTY
K-Number: K942314 · 1994-06-02
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Device Summary
Frequently Asked Questions
What is the LORREX GAUZE SPONGES SPECIALTY?
LORREX GAUZE SPONGES SPECIALTY is a medical device that received FDA 510(k) clearance on 1994-06-02. The listed applicant is Lorrex Health Products. The 510(k) number is K942314.
When did LORREX GAUZE SPONGES SPECIALTY receive FDA 510(k) clearance?
LORREX GAUZE SPONGES SPECIALTY received FDA 510(k) clearance on 1994-06-02, under 510(k) number K942314.
Who is the listed applicant for LORREX GAUZE SPONGES SPECIALTY?
The FDA 510(k) record lists Lorrex Health Products as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LORREX GAUZE SPONGES SPECIALTY?
The FDA product code for LORREX GAUZE SPONGES SPECIALTY 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 Lorrex Health Products 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.
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