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FDA 510(k)

STEIGER TUNNELING INSTRUMENT 285

K-Number: K840529 · 1984-03-12

ApplicantEvermed, Inc.
Decision Date1984-03-12
Product CodeDRC
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

STEIGER TUNNELING INSTRUMENT 285 is the device name listed in this FDA 510(k) record. The listed applicant is Evermed, Inc.. It received FDA 510(k) clearance on 1984-03-12 under 510(k) number K840529. The device is classified under product code DRC. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STEIGER TUNNELING INSTRUMENT 285?

STEIGER TUNNELING INSTRUMENT 285 is a medical device that received FDA 510(k) clearance on 1984-03-12. The listed applicant is Evermed, Inc.. The 510(k) number is K840529.

When did STEIGER TUNNELING INSTRUMENT 285 receive FDA 510(k) clearance?

STEIGER TUNNELING INSTRUMENT 285 received FDA 510(k) clearance on 1984-03-12, under 510(k) number K840529.

Who is the listed applicant for STEIGER TUNNELING INSTRUMENT 285?

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

What is the FDA product code for STEIGER TUNNELING INSTRUMENT 285?

The FDA product code for STEIGER TUNNELING INSTRUMENT 285 is DRC.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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