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FDA 510(k)

PENTAD VOCALIZER

K-Number: K842535 · 1984-07-13

ApplicantPentad Corp.
Decision Date1984-07-13
Product CodeILQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PENTAD VOCALIZER is the device name listed in this FDA 510(k) record. The listed applicant is Pentad Corp.. It received FDA 510(k) clearance on 1984-07-13 under 510(k) number K842535. 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 PENTAD VOCALIZER?

PENTAD VOCALIZER is a medical device that received FDA 510(k) clearance on 1984-07-13. The listed applicant is Pentad Corp.. The 510(k) number is K842535.

When did PENTAD VOCALIZER receive FDA 510(k) clearance?

PENTAD VOCALIZER received FDA 510(k) clearance on 1984-07-13, under 510(k) number K842535.

Who is the listed applicant for PENTAD VOCALIZER?

The FDA 510(k) record lists Pentad Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PENTAD VOCALIZER?

The FDA product code for PENTAD VOCALIZER is ILQ.

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.

Related Devices (Code: ILQ)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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