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FDA 510(k)

DISPOSABLE SPECIALTY SPONGES (DISSECTORS)/MODIFIED

K-Number: K913302 · 1992-07-23

ApplicantCarwild Corp.
Decision Date1992-07-23
Product CodeGDY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE SPECIALTY SPONGES (DISSECTORS)/MODIFIED is the device name listed in this FDA 510(k) record. The listed applicant is Carwild Corp.. It received FDA 510(k) clearance on 1992-07-23 under 510(k) number K913302. The device is classified under product code GDY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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

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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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