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FDA 510(k)

BODAI PATIENT COMMUNICATOR

K-Number: K812720 · 1981-11-05

ApplicantSontek Industries, Inc.
Decision Date1981-11-05
Product CodeILQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

BODAI PATIENT COMMUNICATOR is the device name listed in this FDA 510(k) record. The listed applicant is Sontek Industries, Inc.. It received FDA 510(k) clearance on 1981-11-05 under 510(k) number K812720. The device is classified under product code ILQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BODAI PATIENT COMMUNICATOR?

BODAI PATIENT COMMUNICATOR is a medical device that received FDA 510(k) clearance on 1981-11-05. The listed applicant is Sontek Industries, Inc.. The 510(k) number is K812720.

When did BODAI PATIENT COMMUNICATOR receive FDA 510(k) clearance?

BODAI PATIENT COMMUNICATOR received FDA 510(k) clearance on 1981-11-05, under 510(k) number K812720.

Who is the listed applicant for BODAI PATIENT COMMUNICATOR?

The FDA 510(k) record lists Sontek Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BODAI PATIENT COMMUNICATOR?

The FDA product code for BODAI PATIENT COMMUNICATOR is ILQ.

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Other records listing Sontek Industries, Inc. 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.

K833374BITE-BLOCKK833373BODIA BRONCH-SAF DOUBLE SWIVELK833372BODIA TRACH-SAF DOUBLE SWIVELK833361TUBE-TITLEK813324BODAI SWIVEL YK811241BODAI SUCTION -SAFE 4

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Related Devices (Code: ILQ)

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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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