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FDA 510(k)

HEYER-SCHULTE HERMETIC EXTERNAL CSF DRAIN. SYSTEM

K-Number: K864676 · 1986-12-29

ApplicantAmerican V. Mueller
Decision Date1986-12-29
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

HEYER-SCHULTE HERMETIC EXTERNAL CSF DRAIN. SYSTEM 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 1986-12-29 under 510(k) number K864676. The device is classified under product code JXG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEYER-SCHULTE HERMETIC EXTERNAL CSF DRAIN. SYSTEM?

HEYER-SCHULTE HERMETIC EXTERNAL CSF DRAIN. SYSTEM is a medical device that received FDA 510(k) clearance on 1986-12-29. The listed applicant is American V. Mueller. The 510(k) number is K864676.

When did HEYER-SCHULTE HERMETIC EXTERNAL CSF DRAIN. SYSTEM receive FDA 510(k) clearance?

HEYER-SCHULTE HERMETIC EXTERNAL CSF DRAIN. SYSTEM received FDA 510(k) clearance on 1986-12-29, under 510(k) number K864676.

Who is the listed applicant for HEYER-SCHULTE HERMETIC EXTERNAL CSF DRAIN. SYSTEM?

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 HEYER-SCHULTE HERMETIC EXTERNAL CSF DRAIN. SYSTEM?

The FDA product code for HEYER-SCHULTE HERMETIC EXTERNAL CSF DRAIN. SYSTEM is JXG.

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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 SYSK862772V. MUELLER (R) GOOSENECK CIRCULAR STAPLERK861471V. MUELLER VITAL CLIP-HEMOSTATIC CLIPK854568V. MUELLER PNEUMO-INTESTINAL 15 VASCULAR & 30 STAP

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Related Devices (Code: JXG)

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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