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FDA 510(k)

THE EXTRACTOR I TM

K-Number: K801327 · 1980-06-09

ApplicantThe Anspach Effort, Inc.
Decision Date1980-06-09
Product CodeHWB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

THE EXTRACTOR I TM is the device name listed in this FDA 510(k) record. The listed applicant is The Anspach Effort, Inc.. It received FDA 510(k) clearance on 1980-06-09 under 510(k) number K801327. The device is classified under product code HWB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE EXTRACTOR I TM?

THE EXTRACTOR I TM is a medical device that received FDA 510(k) clearance on 1980-06-09. The listed applicant is The Anspach Effort, Inc.. The 510(k) number is K801327.

When did THE EXTRACTOR I TM receive FDA 510(k) clearance?

THE EXTRACTOR I TM received FDA 510(k) clearance on 1980-06-09, under 510(k) number K801327.

Who is the listed applicant for THE EXTRACTOR I TM?

The FDA 510(k) record lists The Anspach Effort, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for THE EXTRACTOR I TM?

The FDA product code for THE EXTRACTOR I TM is HWB.

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Other records listing The Anspach Effort, Inc. 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.

K220485Wireless Hand Control, EG1A (WIRELESS-HC), Receiver for Wireless Hand Control, EG1A (RECEIVER-HC)K183545Anspach Helix Dissection ToolsK180063OCM-G1 AttachmentK131053ANSPACH XMAX, EMAX2 AND EMAX2 PLUS SYSTEM WITH OTOLOGIC ATTACHMENT SYSTEMK113476ANSPACH DISSECTION TOOLSK082637CRANIAL PERFORATOR

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Related Devices (Code: HWB)

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.

K873710MAGNETIC RETRIEVER, 1.7MM W/LUER FITTING TM-1350Arthropedics, Inc.K870844SCHULTZ PROSTHESIS COMPONENT INSERTER EXTRACTORWarsaw Orthopedic, Inc.K870083FERRAY EXTRACTORTerray Manufacturing, Inc.K780300HIP PLATE REMOVAL INSTRUMENTRichard'S Medical Equip., Inc.

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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