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FDA 510(k)

IPOS G.L.P. SYSTEM

K-Number: K833868 · 1983-11-28

ApplicantIpos Luneburg
Decision Date1983-11-28
Product CodeKFX
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

IPOS G.L.P. SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Ipos Luneburg. It received FDA 510(k) clearance on 1983-11-28 under 510(k) number K833868. The device is classified under product code KFX. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IPOS G.L.P. SYSTEM?

IPOS G.L.P. SYSTEM is a medical device that received FDA 510(k) clearance on 1983-11-28. The listed applicant is Ipos Luneburg. The 510(k) number is K833868.

When did IPOS G.L.P. SYSTEM receive FDA 510(k) clearance?

IPOS G.L.P. SYSTEM received FDA 510(k) clearance on 1983-11-28, under 510(k) number K833868.

Who is the listed applicant for IPOS G.L.P. SYSTEM?

The FDA 510(k) record lists Ipos Luneburg as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IPOS G.L.P. SYSTEM?

The FDA product code for IPOS G.L.P. SYSTEM is KFX.

Related Clinical Trials

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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Other records listing Ipos Luneburg 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.

K834143NYLON COMPRESSION STUMP SHEATHK831690IPOS ANTI-ADDUCTUS SHOEK802976CARBONACRYLK802977IPOCARBON STRETCH STOCKINETTEK800749IPOCON 7K800716ORTHOTIC LEG GAIT CORRECTOR DEVICE

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Related Devices (Code: KFX)

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.

K932184STERILE LEMAITRE GLOW 'N TELL TAPEVascutech, Inc.K830285REGNELL HYDRAULIC FEMORAL PROTHESISBesco Financial ServiceK822240ETHYLENE OXIDE STERILIZ. PARAMETRIC REL.American Mcgaw

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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