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FDA 510(k)

INSTAPACS/INSTARISPACS

K-Number: K120718 · 2012-04-19

ApplicantMeddiff Technologies Pvt. , Ltd.
Decision Date2012-04-19
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

INSTAPACS/INSTARISPACS 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 2012-04-19 under 510(k) number K120718. 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 INSTAPACS/INSTARISPACS?

INSTAPACS/INSTARISPACS is a medical device that received FDA 510(k) clearance on 2012-04-19. The listed applicant is Meddiff Technologies Pvt. , Ltd.. The 510(k) number is K120718.

When did INSTAPACS/INSTARISPACS receive FDA 510(k) clearance?

INSTAPACS/INSTARISPACS received FDA 510(k) clearance on 2012-04-19, under 510(k) number K120718.

Who is the listed applicant for INSTAPACS/INSTARISPACS?

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 INSTAPACS/INSTARISPACS?

The FDA product code for INSTAPACS/INSTARISPACS is LLZ.

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Other records listing Meddiff Technologies Pvt. , Ltd. 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.

K182572InstaRISPACS / InstaZFP / InstaMobi v5.0

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

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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