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FDA 510(k)

TUBES, LUKENS, TOMAS

K-Number: K781234 · 1978-08-10

ApplicantLudwig Medical, Inc.
Decision Date1978-08-10
Product CodeKDQ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

TUBES, LUKENS, TOMAS is the device name listed in this FDA 510(k) record. The listed applicant is Ludwig Medical, Inc.. It received FDA 510(k) clearance on 1978-08-10 under 510(k) number K781234. The device is classified under product code KDQ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUBES, LUKENS, TOMAS?

TUBES, LUKENS, TOMAS is a medical device that received FDA 510(k) clearance on 1978-08-10. The listed applicant is Ludwig Medical, Inc.. The 510(k) number is K781234.

When did TUBES, LUKENS, TOMAS receive FDA 510(k) clearance?

TUBES, LUKENS, TOMAS received FDA 510(k) clearance on 1978-08-10, under 510(k) number K781234.

Who is the listed applicant for TUBES, LUKENS, TOMAS?

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

What is the FDA product code for TUBES, LUKENS, TOMAS?

The FDA product code for TUBES, LUKENS, TOMAS is KDQ.

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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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