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FDA 510(k)

POWER SCAN 1000

K-Number: K910802 · 1991-05-09

ApplicantWebb Research, Inc.
Decision Date1991-05-09
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

POWER SCAN 1000 is the device name listed in this FDA 510(k) record. The listed applicant is Webb Research, Inc.. It received FDA 510(k) clearance on 1991-05-09 under 510(k) number K910802. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POWER SCAN 1000?

POWER SCAN 1000 is a medical device that received FDA 510(k) clearance on 1991-05-09. The listed applicant is Webb Research, Inc.. The 510(k) number is K910802.

When did POWER SCAN 1000 receive FDA 510(k) clearance?

POWER SCAN 1000 received FDA 510(k) clearance on 1991-05-09, under 510(k) number K910802.

Who is the listed applicant for POWER SCAN 1000?

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

What is the FDA product code for POWER SCAN 1000?

The FDA product code for POWER SCAN 1000 is LNH.

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 Webb Research, 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.

K950980FAST FIND GRID

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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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