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FDA 510(k)

ABDOMINAL BINDER

K-Number: K823663 · 1982-12-30

ApplicantWarm & Form, Orthopedic Materials
Decision Date1982-12-30
Product CodeKTD
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ABDOMINAL BINDER is the device name listed in this FDA 510(k) record. The listed applicant is Warm & Form, Orthopedic Materials. It received FDA 510(k) clearance on 1982-12-30 under 510(k) number K823663. The device is classified under product code KTD. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ABDOMINAL BINDER?

ABDOMINAL BINDER is a medical device that received FDA 510(k) clearance on 1982-12-30. The listed applicant is Warm & Form, Orthopedic Materials. The 510(k) number is K823663.

When did ABDOMINAL BINDER receive FDA 510(k) clearance?

ABDOMINAL BINDER received FDA 510(k) clearance on 1982-12-30, under 510(k) number K823663.

Who is the listed applicant for ABDOMINAL BINDER?

The FDA 510(k) record lists Warm & Form, Orthopedic Materials as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ABDOMINAL BINDER?

The FDA product code for ABDOMINAL BINDER is KTD.

Related Clinical Trials

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Other records listing Warm & Form, Orthopedic Materials 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.

K830245HEAD HALTERK830244TRACTION ACCESSORIESK830243ABDUCTION PILLOWK830246CAST SHOE, CAST BOOTK823664UNIVERSAL SLING, SLING & SWATHEK823661CLAVICLE SUPPORT

View all 24 devices →

Related Devices (Code: KTD)

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.

K823164ABDOMINAL BINDERWarm & Form, Orthopedic MaterialsK780229ABDOMINAL BELTBiomet, Inc.

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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