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FDA 510(k)

MARTIN CHAIR, MODEL C4S1

K-Number: K080506 · 2008-06-09

ApplicantMartin Manufacturing Co., LLC
Decision Date2008-06-09
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MARTIN CHAIR, MODEL C4S1 is the device name listed in this FDA 510(k) record. The listed applicant is Martin Manufacturing Co., LLC. It received FDA 510(k) clearance on 2008-06-09 under 510(k) number K080506. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MARTIN CHAIR, MODEL C4S1?

MARTIN CHAIR, MODEL C4S1 is a medical device that received FDA 510(k) clearance on 2008-06-09. The listed applicant is Martin Manufacturing Co., LLC. The 510(k) number is K080506.

When did MARTIN CHAIR, MODEL C4S1 receive FDA 510(k) clearance?

MARTIN CHAIR, MODEL C4S1 received FDA 510(k) clearance on 2008-06-09, under 510(k) number K080506.

Who is the listed applicant for MARTIN CHAIR, MODEL C4S1?

The FDA 510(k) record lists Martin Manufacturing Co., LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MARTIN CHAIR, MODEL C4S1?

The FDA product code for MARTIN CHAIR, MODEL C4S1 is IOR.

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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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