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FDA 510(k)

V. MUELLER PNEUMO-INTESTINAL 15 VASCULAR & 30 STAP

K-Number: K854568 · 1985-12-02

ApplicantAmerican V. Mueller
Decision Date1985-12-02
Product CodeGEF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

V. MUELLER PNEUMO-INTESTINAL 15 VASCULAR & 30 STAP 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 1985-12-02 under 510(k) number K854568. The device is classified under product code GEF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the V. MUELLER PNEUMO-INTESTINAL 15 VASCULAR & 30 STAP?

V. MUELLER PNEUMO-INTESTINAL 15 VASCULAR & 30 STAP is a medical device that received FDA 510(k) clearance on 1985-12-02. The listed applicant is American V. Mueller. The 510(k) number is K854568.

When did V. MUELLER PNEUMO-INTESTINAL 15 VASCULAR & 30 STAP receive FDA 510(k) clearance?

V. MUELLER PNEUMO-INTESTINAL 15 VASCULAR & 30 STAP received FDA 510(k) clearance on 1985-12-02, under 510(k) number K854568.

Who is the listed applicant for V. MUELLER PNEUMO-INTESTINAL 15 VASCULAR & 30 STAP?

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 V. MUELLER PNEUMO-INTESTINAL 15 VASCULAR & 30 STAP?

The FDA product code for V. MUELLER PNEUMO-INTESTINAL 15 VASCULAR & 30 STAP is GEF.

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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: GEF)

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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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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