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FDA 510(k)

MULTITUBULAR THORACIC AIR SPLINTS

K-Number: K811750 · 1981-07-20

ApplicantRoger Cestac & Assoc.
Decision Date1981-07-20
Product CodeIPT
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MULTITUBULAR THORACIC AIR SPLINTS 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 1981-07-20 under 510(k) number K811750. The device is classified under product code IPT. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTITUBULAR THORACIC AIR SPLINTS?

MULTITUBULAR THORACIC AIR SPLINTS is a medical device that received FDA 510(k) clearance on 1981-07-20. The listed applicant is Roger Cestac & Assoc.. The 510(k) number is K811750.

When did MULTITUBULAR THORACIC AIR SPLINTS receive FDA 510(k) clearance?

MULTITUBULAR THORACIC AIR SPLINTS received FDA 510(k) clearance on 1981-07-20, under 510(k) number K811750.

Who is the listed applicant for MULTITUBULAR THORACIC AIR SPLINTS?

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 THORACIC AIR SPLINTS?

The FDA product code for MULTITUBULAR THORACIC AIR SPLINTS is IPT.

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.

K811704MULTITUBULAR AIR SPLINT KIT

Related Devices (Code: IPT)

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.

K963091VOLLMAN PRONE POSITIONERHill-Rom, Inc.K821645BACK SKPPORTSFred Sammons, Inc.K812401CRUCIFORM ANTERIOR SPINAL HYPEREXTEN. OSurgical Appliance Industries, Inc.K761128LATERAL TRUNK SUPPORTSFred 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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