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FDA 510(k)

DISPOSABLE SPECIALITY SPONGES

K-Number: K791870 · 1979-11-05

ApplicantCarwild Corp.
Decision Date1979-11-05
Product CodeGDI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE SPECIALITY 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 1979-11-05 under 510(k) number K791870. The device is classified under product code GDI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE SPECIALITY SPONGES?

DISPOSABLE SPECIALITY SPONGES is a medical device that received FDA 510(k) clearance on 1979-11-05. The listed applicant is Carwild Corp.. The 510(k) number is K791870.

When did DISPOSABLE SPECIALITY SPONGES receive FDA 510(k) clearance?

DISPOSABLE SPECIALITY SPONGES received FDA 510(k) clearance on 1979-11-05, under 510(k) number K791870.

Who is the listed applicant for DISPOSABLE SPECIALITY 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 DISPOSABLE SPECIALITY SPONGES?

The FDA product code for DISPOSABLE SPECIALITY SPONGES is GDI.

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.

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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.

K913303LAP SPONGES, MODIFIEDK913302DISPOSABLE SPECIALTY SPONGES (DISSECTORS)/MODIFIEDK833688SUTURE REMOVAL KITS STERILEK791872LAP SPONGESK791871NEUROLOGICAL SPONGES (PATTIES)

Related Devices (Code: GDI)

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.

K896383DISPOSABLE EXTERNAL CLAMPSGalenica Enterprises, Inc.K850288HEPATIC PARENCHYMAL SUCTION DISSECTORBeecher Medical Diagnostic InstrumentationK831912ROUND-BEEHIVE- DISSECTORS 3/8Ormed Mfg., Inc.K822569TYMPANOPLASTY & SKIN DISSECTORSKelleher Corp.K803292FIELD SUCTION DISSECTORV. Mueller O.V. Baxter Healthcare Corp.K791703TEW BYPASS INSTRUMENTS & DISSECTING KITEdward Weck, Inc.

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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