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FDA 510(k)

MEDLINE ELECTRONIC POSITIONING CHAIR

K-Number: K001937 · 2000-09-22

Decision Date2000-09-22
Product CodeINO
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MEDLINE ELECTRONIC POSITIONING CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Medline Industries, Inc.. It received FDA 510(k) clearance on 2000-09-22 under 510(k) number K001937. The device is classified under product code INO. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDLINE ELECTRONIC POSITIONING CHAIR?

MEDLINE ELECTRONIC POSITIONING CHAIR is a medical device that received FDA 510(k) clearance on 2000-09-22. The listed applicant is Medline Industries, Inc.. The 510(k) number is K001937.

When did MEDLINE ELECTRONIC POSITIONING CHAIR receive FDA 510(k) clearance?

MEDLINE ELECTRONIC POSITIONING CHAIR received FDA 510(k) clearance on 2000-09-22, under 510(k) number K001937.

Who is the listed applicant for MEDLINE ELECTRONIC POSITIONING CHAIR?

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

What is the FDA product code for MEDLINE ELECTRONIC POSITIONING CHAIR?

The FDA product code for MEDLINE ELECTRONIC POSITIONING CHAIR is INO.

Related Clinical Trials

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.

Other records listing Medline Industries, 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.

View all 223 devices →

Related Devices (Code: INO)

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.

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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