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FDA 510(k)

EXTENDO-BAC TABLE

K-Number: K914769 · 1992-01-08

ApplicantReinert Technics, Inc.
Decision Date1992-01-08
Product CodeINW
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

EXTENDO-BAC TABLE is the device name listed in this FDA 510(k) record. The listed applicant is Reinert Technics, Inc.. It received FDA 510(k) clearance on 1992-01-08 under 510(k) number K914769. The device is classified under product code INW. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EXTENDO-BAC TABLE?

EXTENDO-BAC TABLE is a medical device that received FDA 510(k) clearance on 1992-01-08. The listed applicant is Reinert Technics, Inc.. The 510(k) number is K914769.

When did EXTENDO-BAC TABLE receive FDA 510(k) clearance?

EXTENDO-BAC TABLE received FDA 510(k) clearance on 1992-01-08, under 510(k) number K914769.

Who is the listed applicant for EXTENDO-BAC TABLE?

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

What is the FDA product code for EXTENDO-BAC TABLE?

The FDA product code for EXTENDO-BAC TABLE is INW.

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Related Devices (Code: INW)

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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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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