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FDA 510(k)

InstaRISPACS / InstaZFP / InstaMobi v5.0

K-Number: K182572 · 2019-04-12

ApplicantMeddiff Technologies Pvt. , Ltd.
Decision Date2019-04-12
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

InstaRISPACS / InstaZFP / InstaMobi v5.0 is the device name listed in this FDA 510(k) record. The listed applicant is Meddiff Technologies Pvt. , Ltd.. It received FDA 510(k) clearance on 2019-04-12 under 510(k) number K182572. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the InstaRISPACS / InstaZFP / InstaMobi v5.0?

InstaRISPACS / InstaZFP / InstaMobi v5.0 is a medical device that received FDA 510(k) clearance on 2019-04-12. The listed applicant is Meddiff Technologies Pvt. , Ltd.. The 510(k) number is K182572.

When did InstaRISPACS / InstaZFP / InstaMobi v5.0 receive FDA 510(k) clearance?

InstaRISPACS / InstaZFP / InstaMobi v5.0 received FDA 510(k) clearance on 2019-04-12, under 510(k) number K182572.

Who is the listed applicant for InstaRISPACS / InstaZFP / InstaMobi v5.0?

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

What is the FDA product code for InstaRISPACS / InstaZFP / InstaMobi v5.0?

The FDA product code for InstaRISPACS / InstaZFP / InstaMobi v5.0 is LLZ.

Related Devices (Code: LLZ)

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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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.

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