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FDA 510(k)

HEYER-SCHULTE SPETZLER LUMBAR-PERITONEAL SHUNT SYS

K-Number: K871685 · 1987-06-12

ApplicantAmerican V. Mueller
Decision Date1987-06-12
Product CodeJXG
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

HEYER-SCHULTE SPETZLER LUMBAR-PERITONEAL SHUNT SYS 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 1987-06-12 under 510(k) number K871685. 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 SPETZLER LUMBAR-PERITONEAL SHUNT SYS?

HEYER-SCHULTE SPETZLER LUMBAR-PERITONEAL SHUNT SYS is a medical device that received FDA 510(k) clearance on 1987-06-12. The listed applicant is American V. Mueller. The 510(k) number is K871685.

When did HEYER-SCHULTE SPETZLER LUMBAR-PERITONEAL SHUNT SYS receive FDA 510(k) clearance?

HEYER-SCHULTE SPETZLER LUMBAR-PERITONEAL SHUNT SYS received FDA 510(k) clearance on 1987-06-12, under 510(k) number K871685.

Who is the listed applicant for HEYER-SCHULTE SPETZLER LUMBAR-PERITONEAL SHUNT SYS?

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 SPETZLER LUMBAR-PERITONEAL SHUNT SYS?

The FDA product code for HEYER-SCHULTE SPETZLER LUMBAR-PERITONEAL SHUNT SYS 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 SYSTEMK864676HEYER-SCHULTE HERMETIC EXTERNAL CSF DRAIN. SYSTEMK862772V. 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.

K261004Codman® Distal Peritoneal Catheter, Barium Open End (82-1682); Codman® HOLTER® Peritoneal Catheter (SALMON Design) (82-1684)Integra Lifesciences Production CorporationK251598IntellidropBrainspace, Inc.K250636Sophy Mini Monopressure Valve (SM1)SophysaK252514EVAC-MRIPhasor Health, LLCK243531Codman Libertís Shunt Catheter with Bactiseal and Endexo TechnologyIntegra Lifesciences Production CorporationK243552Codman Libertís™ 1.5 mm EVD Catheter with Bactiseal® and Endexo® Technology with Luer Connection (821761); Codman Libertís™ 1.9 mm EVD Catheter with Bactiseal® and Endexo® Technology with Luer Connection (821762)Integra Lifesciences Production Corporation

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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