FDA 510(k)

EX N' FLEX EF-200

K-Number: K925270 · 1993-07-21

Decision Date1993-07-21

Product CodeBXB

Advisory CommitteePM

DecisionSubstantially Equivalent

Device Summary

EX N' FLEX EF-200 is the device name listed in this FDA 510(k) record. The listed applicant is Tecogics Scientific , Ltd.. It received FDA 510(k) clearance on 1993-07-21 under 510(k) number K925270. The device is classified under product code BXB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EX N' FLEX EF-200?

EX N' FLEX EF-200 is a medical device that received FDA 510(k) clearance on 1993-07-21. The listed applicant is Tecogics Scientific , Ltd.. The 510(k) number is K925270.

When did EX N' FLEX EF-200 receive FDA 510(k) clearance?

EX N' FLEX EF-200 received FDA 510(k) clearance on 1993-07-21, under 510(k) number K925270.

Who is the listed applicant for EX N' FLEX EF-200?

The FDA 510(k) record lists Tecogics Scientific , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EX N' FLEX EF-200?

The FDA product code for EX N' FLEX EF-200 is BXB.

Related Devices (Code: BXB)

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.

K072887G-TRAINER MEDICALAlter-G, Inc.K003272FLO-BOOTDiscovery Group, LLC K952975ANKLE CALF EXERCISER PHLEBOPUMPPrevent Products, Inc.K953456E-Z FLEXFluid Motion Biotechnologies, Inc.K955105BTE CPM-10Baltimore Therapeutic Equipment Co.K955106BTE CPM-20Baltimore Therapeutic Equipment Co.

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.