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FDA 510(k)

VARIOUS TEMPLATE APPLICATORS

K-Number: K910862 · 1991-04-18

Decision Date1991-04-18
Product CodeIWJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VARIOUS TEMPLATE APPLICATORS is the device name listed in this FDA 510(k) record. The listed applicant is Best Industries. It received FDA 510(k) clearance on 1991-04-18 under 510(k) number K910862. The device is classified under product code IWJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VARIOUS TEMPLATE APPLICATORS?

VARIOUS TEMPLATE APPLICATORS is a medical device that received FDA 510(k) clearance on 1991-04-18. The listed applicant is Best Industries. The 510(k) number is K910862.

When did VARIOUS TEMPLATE APPLICATORS receive FDA 510(k) clearance?

VARIOUS TEMPLATE APPLICATORS received FDA 510(k) clearance on 1991-04-18, under 510(k) number K910862.

Who is the listed applicant for VARIOUS TEMPLATE APPLICATORS?

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

What is the FDA product code for VARIOUS TEMPLATE APPLICATORS?

The FDA product code for VARIOUS TEMPLATE APPLICATORS is IWJ.

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 Best Industries 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 9 devices →

Related Devices (Code: IWJ)

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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