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FDA 510(k)

CONTRAST SENSITIVITY EQUIPMENT

K-Number: K830770 · 1983-04-28

ApplicantCadwell Laboratories, Inc.
Decision Date1983-04-28
Product CodeHLX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CONTRAST SENSITIVITY EQUIPMENT is the device name listed in this FDA 510(k) record. The listed applicant is Cadwell Laboratories, Inc.. It received FDA 510(k) clearance on 1983-04-28 under 510(k) number K830770. The device is classified under product code HLX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTRAST SENSITIVITY EQUIPMENT?

CONTRAST SENSITIVITY EQUIPMENT is a medical device that received FDA 510(k) clearance on 1983-04-28. The listed applicant is Cadwell Laboratories, Inc.. The 510(k) number is K830770.

When did CONTRAST SENSITIVITY EQUIPMENT receive FDA 510(k) clearance?

CONTRAST SENSITIVITY EQUIPMENT received FDA 510(k) clearance on 1983-04-28, under 510(k) number K830770.

Who is the listed applicant for CONTRAST SENSITIVITY EQUIPMENT?

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

What is the FDA product code for CONTRAST SENSITIVITY EQUIPMENT?

The FDA product code for CONTRAST SENSITIVITY EQUIPMENT is HLX.

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Other records listing Cadwell Laboratories, 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.

K061706CADWELL EASYNET OXIMETER MODULEK061705CADWELL EASYNET NASAL PRESSURE MODULEK042350TES-1 CONSTANT VOLTAGE ELECTRICAL STIMULATORK040986CADWELL LIMB MOVEMENT MODULEK040932EASYNET BODY POSITION MODULEK971214KILOWIN

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Related Devices (Code: HLX)

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.

K003442MODIFICATION TO EDI VERIS SYSTEMElectro-Diagnostic Imaging, Inc.K983983EDI VERIS SYSTEMElectro-Diagnostic Imaging, Inc.K925741CLARUS ENDOSCOPIC HOOK KNIFEClarus Medical Systems, Inc.K914393RETINA TESTERRetina TesterK914163SCOPTOPIC SENSITIVITY TEST-1[SST-1]Lkc Technologies, Inc.K873990IRAS EDS INTERFEROMETRIC STIMULATORRandwal Instrument Co., 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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