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FDA 510(k)

MEDICAL DEPOT-WHEELCHAIRS, MODEL SENTRA,ASTAIRE AND VIPER

K-Number: K003783 · 2001-01-12

Decision Date2001-01-12
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MEDICAL DEPOT-WHEELCHAIRS, MODEL SENTRA,ASTAIRE AND VIPER is the device name listed in this FDA 510(k) record. The listed applicant is Medical Depot, Inc.. It received FDA 510(k) clearance on 2001-01-12 under 510(k) number K003783. 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 MEDICAL DEPOT-WHEELCHAIRS, MODEL SENTRA,ASTAIRE AND VIPER?

MEDICAL DEPOT-WHEELCHAIRS, MODEL SENTRA,ASTAIRE AND VIPER is a medical device that received FDA 510(k) clearance on 2001-01-12. The listed applicant is Medical Depot, Inc.. The 510(k) number is K003783.

When did MEDICAL DEPOT-WHEELCHAIRS, MODEL SENTRA,ASTAIRE AND VIPER receive FDA 510(k) clearance?

MEDICAL DEPOT-WHEELCHAIRS, MODEL SENTRA,ASTAIRE AND VIPER received FDA 510(k) clearance on 2001-01-12, under 510(k) number K003783.

Who is the listed applicant for MEDICAL DEPOT-WHEELCHAIRS, MODEL SENTRA,ASTAIRE AND VIPER?

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

What is the FDA product code for MEDICAL DEPOT-WHEELCHAIRS, MODEL SENTRA,ASTAIRE AND VIPER?

The FDA product code for MEDICAL DEPOT-WHEELCHAIRS, MODEL SENTRA,ASTAIRE AND VIPER is IOR.

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 Medical Depot, 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: IOR)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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