FDA 510(k)

VIEW COM

K-Number: K990759 · 1999-04-15

Decision Date1999-04-15

Product CodeLLZ

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

VIEW COM is the device name listed in this FDA 510(k) record. The listed applicant is Electromed Intl., Ltd.. It received FDA 510(k) clearance on 1999-04-15 under 510(k) number K990759. 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 VIEW COM?

VIEW COM is a medical device that received FDA 510(k) clearance on 1999-04-15. The listed applicant is Electromed Intl., Ltd.. The 510(k) number is K990759.

When did VIEW COM receive FDA 510(k) clearance?

VIEW COM received FDA 510(k) clearance on 1999-04-15, under 510(k) number K990759.

Who is the listed applicant for VIEW COM?

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

What is the FDA product code for VIEW COM?

The FDA product code for VIEW COM is LLZ.

Other records listing Electromed Intl., 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.

K003688VIEW READING STATION K000474VIEW NT K974255CD-R STATION AND VRS-2000 K971176VIEW ARCHIVING STATION K950694COMPACT-X K880050EDEC 60R

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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.