Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

APPENDIX EXTRACTOR 8385.50

K-Number: K940900 · 1994-04-20

Decision Date1994-04-20
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

APPENDIX EXTRACTOR 8385.50 is the device name listed in this FDA 510(k) record. The listed applicant is Richard Wolf Medical Instruments Corp.. It received FDA 510(k) clearance on 1994-04-20 under 510(k) number K940900. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the APPENDIX EXTRACTOR 8385.50?

APPENDIX EXTRACTOR 8385.50 is a medical device that received FDA 510(k) clearance on 1994-04-20. The listed applicant is Richard Wolf Medical Instruments Corp.. The 510(k) number is K940900.

When did APPENDIX EXTRACTOR 8385.50 receive FDA 510(k) clearance?

APPENDIX EXTRACTOR 8385.50 received FDA 510(k) clearance on 1994-04-20, under 510(k) number K940900.

Who is the listed applicant for APPENDIX EXTRACTOR 8385.50?

The FDA 510(k) record lists Richard Wolf Medical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for APPENDIX EXTRACTOR 8385.50?

The FDA product code for APPENDIX EXTRACTOR 8385.50 is GCJ.

Related Clinical Trials

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.

Other records listing Richard Wolf Medical Instruments Corp. 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.

View all 142 devices →

Related Devices (Code: GCJ)

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.

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.

↑