PROTECTIVE RESTRAINT(MODELS #302,440,750 AND A30 X 30 BELT.
K-Number: K972338 · 1997-07-24
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Device Summary
Frequently Asked Questions
What is the PROTECTIVE RESTRAINT(MODELS #302,440,750 AND A30 X 30 BELT.?
PROTECTIVE RESTRAINT(MODELS #302,440,750 AND A30 X 30 BELT. is a medical device that received FDA 510(k) clearance on 1997-07-24. The listed applicant is Geriatric Products, Inc.. The 510(k) number is K972338.
When did PROTECTIVE RESTRAINT(MODELS #302,440,750 AND A30 X 30 BELT. receive FDA 510(k) clearance?
PROTECTIVE RESTRAINT(MODELS #302,440,750 AND A30 X 30 BELT. received FDA 510(k) clearance on 1997-07-24, under 510(k) number K972338.
Who is the listed applicant for PROTECTIVE RESTRAINT(MODELS #302,440,750 AND A30 X 30 BELT.?
The FDA 510(k) record lists Geriatric Products, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROTECTIVE RESTRAINT(MODELS #302,440,750 AND A30 X 30 BELT.?
The FDA product code for PROTECTIVE RESTRAINT(MODELS #302,440,750 AND A30 X 30 BELT. is FMQ.
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.
Related Devices (Code: FMQ)
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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