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FDA 510(k)

PORTABLE LIMB LOAD MONITOR (BMLLM-100)

K-Number: K915326 · 1992-10-20

Decision Date1992-10-20
Product CodeIKE
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PORTABLE LIMB LOAD MONITOR (BMLLM-100) is the device name listed in this FDA 510(k) record. The listed applicant is Bar Med Pty , Ltd.. It received FDA 510(k) clearance on 1992-10-20 under 510(k) number K915326. The device is classified under product code IKE. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PORTABLE LIMB LOAD MONITOR (BMLLM-100)?

PORTABLE LIMB LOAD MONITOR (BMLLM-100) is a medical device that received FDA 510(k) clearance on 1992-10-20. The listed applicant is Bar Med Pty , Ltd.. The 510(k) number is K915326.

When did PORTABLE LIMB LOAD MONITOR (BMLLM-100) receive FDA 510(k) clearance?

PORTABLE LIMB LOAD MONITOR (BMLLM-100) received FDA 510(k) clearance on 1992-10-20, under 510(k) number K915326.

Who is the listed applicant for PORTABLE LIMB LOAD MONITOR (BMLLM-100)?

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

What is the FDA product code for PORTABLE LIMB LOAD MONITOR (BMLLM-100)?

The FDA product code for PORTABLE LIMB LOAD MONITOR (BMLLM-100) is IKE.

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.

Related Devices (Code: IKE)

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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