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FDA 510(k)

CIRCLE NEPHROSTOMY TUBE INTRODUCER

K-Number: K810533 · 1981-03-11

ApplicantAmerican V. Mueller
Decision Date1981-03-11
Product CodeKOA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

CIRCLE NEPHROSTOMY TUBE INTRODUCER 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 1981-03-11 under 510(k) number K810533. The device is classified under product code KOA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CIRCLE NEPHROSTOMY TUBE INTRODUCER?

CIRCLE NEPHROSTOMY TUBE INTRODUCER is a medical device that received FDA 510(k) clearance on 1981-03-11. The listed applicant is American V. Mueller. The 510(k) number is K810533.

When did CIRCLE NEPHROSTOMY TUBE INTRODUCER receive FDA 510(k) clearance?

CIRCLE NEPHROSTOMY TUBE INTRODUCER received FDA 510(k) clearance on 1981-03-11, under 510(k) number K810533.

Who is the listed applicant for CIRCLE NEPHROSTOMY TUBE INTRODUCER?

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 CIRCLE NEPHROSTOMY TUBE INTRODUCER?

The FDA product code for CIRCLE NEPHROSTOMY TUBE INTRODUCER is KOA.

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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: KOA)

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.

K182664FiXcisionAgency For Medical Innovations GmbHK950267URETHRAL SUTURE GUIDEApplied Medical ResourcesK932465LI VASECTOMYFemcare , Ltd.K921546VASOVASOSTOMY SETCook Urological, Inc.K931181VESITEC SUTURE PASSERVesitec Medical, Inc.K921304DDV LIGATORNorth American 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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