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FDA 510(k)

ABDUCTION PILLOW

K-Number: K830243 · 1983-03-08

ApplicantWarm & Form, Orthopedic Materials
Decision Date1983-03-08
Product CodeIOZ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

ABDUCTION PILLOW 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 1983-03-08 under 510(k) number K830243. The device is classified under product code IOZ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ABDUCTION PILLOW?

ABDUCTION PILLOW is a medical device that received FDA 510(k) clearance on 1983-03-08. The listed applicant is Warm & Form, Orthopedic Materials. The 510(k) number is K830243.

When did ABDUCTION PILLOW receive FDA 510(k) clearance?

ABDUCTION PILLOW received FDA 510(k) clearance on 1983-03-08, under 510(k) number K830243.

Who is the listed applicant for ABDUCTION PILLOW?

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 ABDUCTION PILLOW?

The FDA product code for ABDUCTION PILLOW is IOZ.

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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 ACCESSORIESK830246CAST SHOE, CAST BOOTK823661CLAVICLE SUPPORTK823663ABDOMINAL BINDERK823667CERVICAL COLLAR

View all 24 devices →

Related Devices (Code: IOZ)

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.

K823820ABDUCTION PILLOWDanek Medical, Inc.K810557HIP ABDUCTION SPLINTOrthomedicsK780375PAVLIK HARNESSBiomet, 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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