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FDA 510(k)

MODEL L-2000 & L-500 CHIROPRACTIC TABLES

K-Number: K885276 · 1989-04-26

ApplicantLesarn Mfg., Ltd.
Decision Date1989-04-26
Product CodeINQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MODEL L-2000 & L-500 CHIROPRACTIC TABLES is the device name listed in this FDA 510(k) record. The listed applicant is Lesarn Mfg., Ltd.. It received FDA 510(k) clearance on 1989-04-26 under 510(k) number K885276. The device is classified under product code INQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL L-2000 & L-500 CHIROPRACTIC TABLES?

MODEL L-2000 & L-500 CHIROPRACTIC TABLES is a medical device that received FDA 510(k) clearance on 1989-04-26. The listed applicant is Lesarn Mfg., Ltd.. The 510(k) number is K885276.

When did MODEL L-2000 & L-500 CHIROPRACTIC TABLES receive FDA 510(k) clearance?

MODEL L-2000 & L-500 CHIROPRACTIC TABLES received FDA 510(k) clearance on 1989-04-26, under 510(k) number K885276.

Who is the listed applicant for MODEL L-2000 & L-500 CHIROPRACTIC TABLES?

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

What is the FDA product code for MODEL L-2000 & L-500 CHIROPRACTIC TABLES?

The FDA product code for MODEL L-2000 & L-500 CHIROPRACTIC TABLES is INQ.

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Related Devices (Code: INQ)

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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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