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FDA 510(k)

MULTITUBULAR AIR SPLINT KIT

K-Number: K811704 · 1981-07-01

ApplicantRoger Cestac & Assoc.
Decision Date1981-07-01
Product CodeIQI
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MULTITUBULAR AIR SPLINT KIT is the device name listed in this FDA 510(k) record. The listed applicant is Roger Cestac & Assoc.. It received FDA 510(k) clearance on 1981-07-01 under 510(k) number K811704. The device is classified under product code IQI. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTITUBULAR AIR SPLINT KIT?

MULTITUBULAR AIR SPLINT KIT is a medical device that received FDA 510(k) clearance on 1981-07-01. The listed applicant is Roger Cestac & Assoc.. The 510(k) number is K811704.

When did MULTITUBULAR AIR SPLINT KIT receive FDA 510(k) clearance?

MULTITUBULAR AIR SPLINT KIT received FDA 510(k) clearance on 1981-07-01, under 510(k) number K811704.

Who is the listed applicant for MULTITUBULAR AIR SPLINT KIT?

The FDA 510(k) record lists Roger Cestac & Assoc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTITUBULAR AIR SPLINT KIT?

The FDA product code for MULTITUBULAR AIR SPLINT KIT is IQI.

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.

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Other records listing Roger Cestac & Assoc. 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.

K811750MULTITUBULAR THORACIC AIR SPLINTS

Related Devices (Code: IQI)

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.

K052771SENSOR WALKOtto Bock Healthcare LPK031576SPARTAN ORTHOPAEDIC WRIST BRACE, MODEL SCT-1Surgitech, Inc.K926391ACCUFLEX DYNAMIC ELBOW ORTHOSISRegulatory & Marketing Services, Inc.K910974MCCONNELL SHOULDER BRACEMcconnell OrthopedicK874502GAIT-AID ORTHOPEDIC INSOLEGait-Aid, Inc.K831542ADJUSTABLE POLYCENTRIC ELBOW HINGEFred Sammons, 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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