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FDA 510(k)

LAP SPONGES

K-Number: K791872 · 1979-11-13

ApplicantCarwild Corp.
Decision Date1979-11-13
Product CodeEFQ
DecisionSubstantially Equivalent

Device Summary

LAP SPONGES is the device name listed in this FDA 510(k) record. The listed applicant is Carwild Corp.. It received FDA 510(k) clearance on 1979-11-13 under 510(k) number K791872. The device is classified under product code EFQ. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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