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FDA 510(k)

LEATHER VALVE CUTTER

K-Number: K831455 · 1983-07-07

ApplicantAmerican V. Mueller
Decision Date1983-07-07
Product CodeDWS
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

LEATHER VALVE CUTTER 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 1983-07-07 under 510(k) number K831455. The device is classified under product code DWS. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEATHER VALVE CUTTER?

LEATHER VALVE CUTTER is a medical device that received FDA 510(k) clearance on 1983-07-07. The listed applicant is American V. Mueller. The 510(k) number is K831455.

When did LEATHER VALVE CUTTER receive FDA 510(k) clearance?

LEATHER VALVE CUTTER received FDA 510(k) clearance on 1983-07-07, under 510(k) number K831455.

Who is the listed applicant for LEATHER VALVE CUTTER?

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 LEATHER VALVE CUTTER?

The FDA product code for LEATHER VALVE CUTTER is DWS.

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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: DWS)

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.

K022238MYOCARDIAL LEAD IMPLANT TOOL, MODEL 10626Medtronic VascularK964445OCTOPUS TISSUE STABILIZER (28001/28002/28003/28004/28005/28006)Dlp, Inc.K962771BURKE CONGENITAL THORACOSCOPY INSTRUMENTSPilling Weck, Inc.K955689RNS STERILE, DISPOSABLE DIGITAL ANGIOGRAPHIC TRAYContour Fabricators of Florida, Inc.K960139G.E. STERILE ANGIOGRAPHIC TRAYGE Medical SystemsK960144G.E. STERILE CT BIOPSY TRAYGE Medical Systems

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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