COMPRESSOGRIP TUBULAR ELASTIC BANDAGE
K-Number: K831551 · 1983-06-07
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Device Summary
Frequently Asked Questions
What is the COMPRESSOGRIP TUBULAR ELASTIC BANDAGE?
COMPRESSOGRIP TUBULAR ELASTIC BANDAGE is a medical device that received FDA 510(k) clearance on 1983-06-07. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K831551.
When did COMPRESSOGRIP TUBULAR ELASTIC BANDAGE receive FDA 510(k) clearance?
COMPRESSOGRIP TUBULAR ELASTIC BANDAGE received FDA 510(k) clearance on 1983-06-07, under 510(k) number K831551.
Who is the listed applicant for COMPRESSOGRIP TUBULAR ELASTIC BANDAGE?
The FDA 510(k) record lists Fred Sammons, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COMPRESSOGRIP TUBULAR ELASTIC BANDAGE?
The FDA product code for COMPRESSOGRIP TUBULAR ELASTIC BANDAGE is FQM.
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 Fred Sammons, 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: FQM)
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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