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FDA 510(k)

SETMA VHT

K-Number: K853163 · 1985-11-05

ApplicantSetma, Inc.
Decision Date1985-11-05
Product CodeILJ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

SETMA VHT is the device name listed in this FDA 510(k) record. The listed applicant is Setma, Inc.. It received FDA 510(k) clearance on 1985-11-05 under 510(k) number K853163. The device is classified under product code ILJ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SETMA VHT?

SETMA VHT is a medical device that received FDA 510(k) clearance on 1985-11-05. The listed applicant is Setma, Inc.. The 510(k) number is K853163.

When did SETMA VHT receive FDA 510(k) clearance?

SETMA VHT received FDA 510(k) clearance on 1985-11-05, under 510(k) number K853163.

Who is the listed applicant for SETMA VHT?

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

What is the FDA product code for SETMA VHT?

The FDA product code for SETMA VHT is ILJ.

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.

Other records listing Setma, 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.

View all 7 devices →

Related Devices (Code: ILJ)

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

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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