DISPOSABLE SPECIALTY SPONGES (DISSECTORS)/MODIFIED
K-Number: K913302 · 1992-07-23
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Device Summary
Frequently Asked Questions
What is the DISPOSABLE SPECIALTY SPONGES (DISSECTORS)/MODIFIED?
DISPOSABLE SPECIALTY SPONGES (DISSECTORS)/MODIFIED is a medical device that received FDA 510(k) clearance on 1992-07-23. The listed applicant is Carwild Corp.. The 510(k) number is K913302.
When did DISPOSABLE SPECIALTY SPONGES (DISSECTORS)/MODIFIED receive FDA 510(k) clearance?
DISPOSABLE SPECIALTY SPONGES (DISSECTORS)/MODIFIED received FDA 510(k) clearance on 1992-07-23, under 510(k) number K913302.
Who is the listed applicant for DISPOSABLE SPECIALTY SPONGES (DISSECTORS)/MODIFIED?
The FDA 510(k) record lists Carwild Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DISPOSABLE SPECIALTY SPONGES (DISSECTORS)/MODIFIED?
The FDA product code for DISPOSABLE SPECIALTY SPONGES (DISSECTORS)/MODIFIED is GDY.
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 Carwild 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: GDY)
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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