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FDA 510(k)

EXTRACTOR III

K-Number: K820292 · 1982-03-02

ApplicantThe Anspach Effort, Inc.
Decision Date1982-03-02
Product Code
DecisionSubstantially Equivalent

Device Summary

EXTRACTOR III 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 1982-03-02 under 510(k) number K820292. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXTRACTOR III?

EXTRACTOR III is a medical device that received FDA 510(k) clearance on 1982-03-02. The listed applicant is The Anspach Effort, Inc.. The 510(k) number is K820292.

When did EXTRACTOR III receive FDA 510(k) clearance?

EXTRACTOR III received FDA 510(k) clearance on 1982-03-02, under 510(k) number K820292.

Who is the listed applicant for EXTRACTOR III?

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

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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

View all 59 devices →

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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