LAP SPONGES
K-Number: K791872 · 1979-11-13
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Device Summary
Frequently Asked Questions
What is the LAP SPONGES?
LAP SPONGES is a medical device that received FDA 510(k) clearance on 1979-11-13. The listed applicant is Carwild Corp.. The 510(k) number is K791872.
When did LAP SPONGES receive FDA 510(k) clearance?
LAP SPONGES received FDA 510(k) clearance on 1979-11-13, under 510(k) number K791872.
Who is the listed applicant for LAP SPONGES?
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 LAP SPONGES?
The FDA product code for LAP 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 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: 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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