NON-STERILE, BULK GAUZE SPONGES
K-Number: K890727 · 1989-03-10
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Device Summary
Frequently Asked Questions
What is the NON-STERILE, BULK GAUZE SPONGES?
NON-STERILE, BULK GAUZE SPONGES is a medical device that received FDA 510(k) clearance on 1989-03-10. The listed applicant is Cypress Medical Products, Ltd.. The 510(k) number is K890727.
When did NON-STERILE, BULK GAUZE SPONGES receive FDA 510(k) clearance?
NON-STERILE, BULK GAUZE SPONGES received FDA 510(k) clearance on 1989-03-10, under 510(k) number K890727.
Who is the listed applicant for NON-STERILE, BULK GAUZE SPONGES?
The FDA 510(k) record lists Cypress Medical Products, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NON-STERILE, BULK GAUZE SPONGES?
The FDA product code for NON-STERILE, BULK GAUZE 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 Cypress Medical Products, 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: 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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