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FDA 510(k)

INSTRUTAINER

K-Number: K844672 · 1985-02-22

ApplicantIntrumed, Inc.
Decision Date1985-02-22
Product CodeFRG
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INSTRUTAINER is the device name listed in this FDA 510(k) record. The listed applicant is Intrumed, Inc.. It received FDA 510(k) clearance on 1985-02-22 under 510(k) number K844672. The device is classified under product code FRG. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSTRUTAINER?

INSTRUTAINER is a medical device that received FDA 510(k) clearance on 1985-02-22. The listed applicant is Intrumed, Inc.. The 510(k) number is K844672.

When did INSTRUTAINER receive FDA 510(k) clearance?

INSTRUTAINER received FDA 510(k) clearance on 1985-02-22, under 510(k) number K844672.

Who is the listed applicant for INSTRUTAINER?

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

What is the FDA product code for INSTRUTAINER?

The FDA product code for INSTRUTAINER is FRG.

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Related Devices (Code: FRG)

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.

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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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