APPENDIX EXTRACTOR 8385.50
K-Number: K940900 · 1994-04-20
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Device Summary
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.
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.
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