EXERCISER, EXTENSOR WAND
K-Number: K770436 · 1977-04-06
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Device Summary
Frequently Asked Questions
What is the EXERCISER, EXTENSOR WAND?
EXERCISER, EXTENSOR WAND is a medical device that received FDA 510(k) clearance on 1977-04-06. The listed applicant is Maddak, Inc.. The 510(k) number is K770436.
When did EXERCISER, EXTENSOR WAND receive FDA 510(k) clearance?
EXERCISER, EXTENSOR WAND received FDA 510(k) clearance on 1977-04-06, under 510(k) number K770436.
Who is the listed applicant for EXERCISER, EXTENSOR WAND?
The FDA 510(k) record lists Maddak, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EXERCISER, EXTENSOR WAND?
The FDA product code for EXERCISER, EXTENSOR WAND is ION.
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 Maddak, 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: ION)
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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