STRETCHPOWER
K-Number: K935188 · 1994-03-24
Device Summary
Frequently Asked Questions
What is the STRETCHPOWER?
STRETCHPOWER is a medical device that received FDA 510(k) clearance on 1994-03-24. The listed applicant is Orthopedic Development, Inc.. The 510(k) number is K935188.
When did STRETCHPOWER receive FDA 510(k) clearance?
STRETCHPOWER received FDA 510(k) clearance on 1994-03-24, under 510(k) number K935188.
Who is the listed applicant for STRETCHPOWER?
The FDA 510(k) record lists Orthopedic Development, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STRETCHPOWER?
The FDA product code for STRETCHPOWER is BXB.
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 Orthopedic Development, 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: 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.
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.