Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

TABLE MAT MORTORIZED/ELECTRIC

K-Number: K940131 · 1994-02-25

Decision Date1994-02-25
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

TABLE MAT MORTORIZED/ELECTRIC is the device name listed in this FDA 510(k) record. The listed applicant is Med Mart, Inc.. It received FDA 510(k) clearance on 1994-02-25 under 510(k) number K940131. The device is classified under product code INQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TABLE MAT MORTORIZED/ELECTRIC?

TABLE MAT MORTORIZED/ELECTRIC is a medical device that received FDA 510(k) clearance on 1994-02-25. The listed applicant is Med Mart, Inc.. The 510(k) number is K940131.

When did TABLE MAT MORTORIZED/ELECTRIC receive FDA 510(k) clearance?

TABLE MAT MORTORIZED/ELECTRIC received FDA 510(k) clearance on 1994-02-25, under 510(k) number K940131.

Who is the listed applicant for TABLE MAT MORTORIZED/ELECTRIC?

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

What is the FDA product code for TABLE MAT MORTORIZED/ELECTRIC?

The FDA product code for TABLE MAT MORTORIZED/ELECTRIC is INQ.

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 Med Mart, 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.

Related Devices (Code: INQ)

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.

↑