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FDA 510(k)

ULTRAPRO MODEL 98

K-Number: K982563 · 1998-10-06

ApplicantRamsoft, Inc.
Decision Date1998-10-06
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

ULTRAPRO MODEL 98 is the device name listed in this FDA 510(k) record. The listed applicant is Ramsoft, Inc.. It received FDA 510(k) clearance on 1998-10-06 under 510(k) number K982563. 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 ULTRAPRO MODEL 98?

ULTRAPRO MODEL 98 is a medical device that received FDA 510(k) clearance on 1998-10-06. The listed applicant is Ramsoft, Inc.. The 510(k) number is K982563.

When did ULTRAPRO MODEL 98 receive FDA 510(k) clearance?

ULTRAPRO MODEL 98 received FDA 510(k) clearance on 1998-10-06, under 510(k) number K982563.

Who is the listed applicant for ULTRAPRO MODEL 98?

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

What is the FDA product code for ULTRAPRO MODEL 98?

The FDA product code for ULTRAPRO MODEL 98 is LLZ.

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Other records listing Ramsoft, Inc. 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.

K222476OmegaAI Image ViewerK052460POWERSERVER, POWERREADER, GATEWAY AND POWERCACHEK031562RAMSOFT PACS, MODEL 3.0K942917ULTRAPRO WORKSTATION

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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