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FDA 510(k)

OB TRIPP TRANSPORT CHAIR

K-Number: K823151 · 1982-11-05

ApplicantOrthion Corp.
Decision Date1982-11-05
Product CodeINM
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

OB TRIPP TRANSPORT CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Orthion Corp.. It received FDA 510(k) clearance on 1982-11-05 under 510(k) number K823151. The device is classified under product code INM. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OB TRIPP TRANSPORT CHAIR?

OB TRIPP TRANSPORT CHAIR is a medical device that received FDA 510(k) clearance on 1982-11-05. The listed applicant is Orthion Corp.. The 510(k) number is K823151.

When did OB TRIPP TRANSPORT CHAIR receive FDA 510(k) clearance?

OB TRIPP TRANSPORT CHAIR received FDA 510(k) clearance on 1982-11-05, under 510(k) number K823151.

Who is the listed applicant for OB TRIPP TRANSPORT CHAIR?

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

What is the FDA product code for OB TRIPP TRANSPORT CHAIR?

The FDA product code for OB TRIPP TRANSPORT CHAIR is INM.

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 Orthion Corp. 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 11 devices →

Related Devices (Code: INM)

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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