FDA 510(k)

LPS 1118

K-Number: K820650 · 1982-04-29

Decision Date1982-04-29

Product CodeKCW

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

LPS 1118 is the device name listed in this FDA 510(k) record. The listed applicant is L.P. Systems Corp.. It received FDA 510(k) clearance on 1982-04-29 under 510(k) number K820650. The device is classified under product code KCW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LPS 1118?

LPS 1118 is a medical device that received FDA 510(k) clearance on 1982-04-29. The listed applicant is L.P. Systems Corp.. The 510(k) number is K820650.

When did LPS 1118 receive FDA 510(k) clearance?

LPS 1118 received FDA 510(k) clearance on 1982-04-29, under 510(k) number K820650.

Who is the listed applicant for LPS 1118?

The FDA 510(k) record lists L.P. Systems Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LPS 1118?

The FDA product code for LPS 1118 is KCW.

Other records listing L.P. Systems Corp. 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.

K945192HAIR REMOVAL SYSTEM

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K954031COMPU-BLEND EPILATORR. A. Fischer Co. Corp.K952611STEREX STERILE DISPOSALE ELECTROLYSIS NEEDLE FOR USE IN EPILATIONSterex Electrolysis Intl., Ltd.K945192HAIR REMOVAL SYSTEML.P. Systems Corp.K943928APILUS ELECTROPILDectro Intl., Inc.K943398THE BLENDTONE ROYALEInstantron K943399THE SS-99Instantron

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.