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FDA 510(k)

MAGNETIC RETRIEVER

K-Number: K854281 · 1985-12-02

ApplicantAspen Laboratories, Inc.
Decision Date1985-12-02
Product Code
DecisionSubstantially Equivalent

Device Summary

MAGNETIC RETRIEVER is the device name listed in this FDA 510(k) record. The listed applicant is Aspen Laboratories, Inc.. It received FDA 510(k) clearance on 1985-12-02 under 510(k) number K854281. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAGNETIC RETRIEVER?

MAGNETIC RETRIEVER is a medical device that received FDA 510(k) clearance on 1985-12-02. The listed applicant is Aspen Laboratories, Inc.. The 510(k) number is K854281.

When did MAGNETIC RETRIEVER receive FDA 510(k) clearance?

MAGNETIC RETRIEVER received FDA 510(k) clearance on 1985-12-02, under 510(k) number K854281.

Who is the listed applicant for MAGNETIC RETRIEVER?

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

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Other records listing Aspen Laboratories, 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.

K981220SYSTEM 7500 ABC ELECTROSURGICAL UNITK963088SHEATH, ELECTROSURGICAL PENCILK955834SYSTEM 6500 ABC ELECTROSURGICAL UNITK9602964000 ETMK953081BEAMER PLUSK953007EXCALIBUR PLUS ELECTROSURGICAL UNIT

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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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