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FDA 510(k)

YARMO NASAL CARTILAGE SOFTENER

K-Number: K812895 · 1981-11-02

ApplicantAmerican V. Mueller
Decision Date1981-11-02
Product CodeKAE
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

YARMO NASAL CARTILAGE SOFTENER is the device name listed in this FDA 510(k) record. The listed applicant is American V. Mueller. It received FDA 510(k) clearance on 1981-11-02 under 510(k) number K812895. The device is classified under product code KAE. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the YARMO NASAL CARTILAGE SOFTENER?

YARMO NASAL CARTILAGE SOFTENER is a medical device that received FDA 510(k) clearance on 1981-11-02. The listed applicant is American V. Mueller. The 510(k) number is K812895.

When did YARMO NASAL CARTILAGE SOFTENER receive FDA 510(k) clearance?

YARMO NASAL CARTILAGE SOFTENER received FDA 510(k) clearance on 1981-11-02, under 510(k) number K812895.

Who is the listed applicant for YARMO NASAL CARTILAGE SOFTENER?

The FDA 510(k) record lists American V. Mueller as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for YARMO NASAL CARTILAGE SOFTENER?

The FDA product code for YARMO NASAL CARTILAGE SOFTENER is KAE.

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Other records listing American V. Mueller 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.

K873771HEYER-SCHULTE(R) ONE PIECE SHUNT VENT. CATH. INTROK873332MAXIVAC(TM) CLOSED WOUND SUCTION DRAINAGE SYSTEMK871685HEYER-SCHULTE SPETZLER LUMBAR-PERITONEAL SHUNT SYSK864676HEYER-SCHULTE HERMETIC EXTERNAL CSF DRAIN. SYSTEMK862772V. MUELLER (R) GOOSENECK CIRCULAR STAPLERK861471V. MUELLER VITAL CLIP-HEMOSTATIC CLIP

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Related Devices (Code: KAE)

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.

K853708LARYNGASCOPES, FORCEPS, MICRO SUCTION TUBE & REFLEDowns Surgical , Ltd.K85179441-180 TO 41-246 VARIOUS NASAL FORCEPSArtiberiaK85177519-790 TO 19-1042 DRESSING/SPONGE FORCEPSArtiberiaK85179541-250 TO 41-282 VARIOUS NASAL CUTTING FORCEPSArtiberiaK833608GOLD ALLIGATOR FORCEPSMicrotek Medical, Inc.K833605CUPPED FORCEPSMicrotek 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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