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FDA 510(k)

LP-5

K-Number: K844179 · 1985-01-18

Decision Date1985-01-18
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LP-5 is the device name listed in this FDA 510(k) record. The listed applicant is Life Products, Inc.. It received FDA 510(k) clearance on 1985-01-18 under 510(k) number K844179. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LP-5?

LP-5 is a medical device that received FDA 510(k) clearance on 1985-01-18. The listed applicant is Life Products, Inc.. The 510(k) number is K844179.

When did LP-5 receive FDA 510(k) clearance?

LP-5 received FDA 510(k) clearance on 1985-01-18, under 510(k) number K844179.

Who is the listed applicant for LP-5?

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

What is the FDA product code for LP-5?

The FDA product code for LP-5 is CBK.

Other records listing Life Products, 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 10 devices →

Related Devices (Code: CBK)

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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