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FDA 510(k)

MICRONET LIGHT DRESSING SPONGE

K-Number: K780408 · 1978-03-22

ApplicantKendall Research Center
Decision Date1978-03-22
Product CodeNAB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MICRONET LIGHT DRESSING SPONGE is the device name listed in this FDA 510(k) record. The listed applicant is Kendall Research Center. It received FDA 510(k) clearance on 1978-03-22 under 510(k) number K780408. The device is classified under product code NAB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRONET LIGHT DRESSING SPONGE?

MICRONET LIGHT DRESSING SPONGE is a medical device that received FDA 510(k) clearance on 1978-03-22. The listed applicant is Kendall Research Center. The 510(k) number is K780408.

When did MICRONET LIGHT DRESSING SPONGE receive FDA 510(k) clearance?

MICRONET LIGHT DRESSING SPONGE received FDA 510(k) clearance on 1978-03-22, under 510(k) number K780408.

Who is the listed applicant for MICRONET LIGHT DRESSING SPONGE?

The FDA 510(k) record lists Kendall Research Center as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICRONET LIGHT DRESSING SPONGE?

The FDA product code for MICRONET LIGHT DRESSING SPONGE is NAB.

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Other records listing Kendall Research Center 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.

K802225TENDER-SORB DRAIN SPONGESK781357T.E.D. SEQUENTIAL COMPRESSION SLEEVESK780062CATHETER/HEMOSTATIC/GERIATRICK780120ANESTHESIA TRAY, CAUDALK772133URINE SPECIMEN COLLECTING DEVICEK772134SYRINGE, IRRIGATION, PRE-FILLED

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Related Devices (Code: NAB)

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.

K946015IVALON EXTERNAL SPONGEIvalonK940755ISOLYER (4X4, 8PLY)Isolyer Co.K931610OMNISORB II, NONWOVEN SPONGE, STERILE AND NONOmni Mfg., Inc.K925590MULTI-TRAUMA DRESSINGGam Industries, Inc.K926072K-BAND AND K-CREPEParema , Ltd.K915591STERILE GAUZE PADSEagle Medical, 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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