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FDA 510(k)

CLEARVIEW

K-Number: K790536 · 1979-03-28

ApplicantHipoint Research, Inc.
Decision Date1979-03-28
Product CodeKXJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CLEARVIEW is the device name listed in this FDA 510(k) record. The listed applicant is Hipoint Research, Inc.. It received FDA 510(k) clearance on 1979-03-28 under 510(k) number K790536. The device is classified under product code KXJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLEARVIEW?

CLEARVIEW is a medical device that received FDA 510(k) clearance on 1979-03-28. The listed applicant is Hipoint Research, Inc.. The 510(k) number is K790536.

When did CLEARVIEW receive FDA 510(k) clearance?

CLEARVIEW received FDA 510(k) clearance on 1979-03-28, under 510(k) number K790536.

Who is the listed applicant for CLEARVIEW?

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

What is the FDA product code for CLEARVIEW?

The FDA product code for CLEARVIEW is KXJ.

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Related Devices (Code: KXJ)

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.

K050190APOLLOVilla Sistemi Medicali S.P.A.K963905RADIOGRAPHIC ITT TABLEX-Ray Technologies, Inc.K955414XRT 400Wuestec Medical, Inc.K951146IMAGING TABLESepta Corp.K950068CARBON FIBER COUCH INSERTMedtec, Inc.K950442INFRARED EXPOSURE HAND SWITCHMedical X-Ray Intl., Inc.

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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