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FDA 510(k)

MODEL 90DX MULTITEST METER

K-Number: K882032 · 1988-08-11

ApplicantMesa Medical, Inc.
Decision Date1988-08-11
Product CodeFLB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODEL 90DX MULTITEST METER is the device name listed in this FDA 510(k) record. The listed applicant is Mesa Medical, Inc.. It received FDA 510(k) clearance on 1988-08-11 under 510(k) number K882032. The device is classified under product code FLB. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 90DX MULTITEST METER?

MODEL 90DX MULTITEST METER is a medical device that received FDA 510(k) clearance on 1988-08-11. The listed applicant is Mesa Medical, Inc.. The 510(k) number is K882032.

When did MODEL 90DX MULTITEST METER receive FDA 510(k) clearance?

MODEL 90DX MULTITEST METER received FDA 510(k) clearance on 1988-08-11, under 510(k) number K882032.

Who is the listed applicant for MODEL 90DX MULTITEST METER?

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

What is the FDA product code for MODEL 90DX MULTITEST METER?

The FDA product code for MODEL 90DX MULTITEST METER is FLB.

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 Mesa Medical, 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.

K92521090DX MULTITEST METER, MODIFICATIONK870811MODEL 102 PH METERK852749RECOMMENDED ALTERNATIVE DIALYZER DISINFECTANTK843520WAREXIN RECOMMENDED ALTERNATIVE DIALYZK834447ECHO MM1000K821383ECHO, MODEL MM-1000

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Related Devices (Code: FLB)

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.

K100237DIALYSATE METER, MODEL D-6Myron L CompanyK92521090DX MULTITEST METER, MODIFICATIONMesa Medical, Inc.K830629COBE RX METERCobe Laboratories, Inc.K821415MODEL 90 BCWestern Laboratories Corp.K770263DIALYSATE METER RS-2100A, CIRCUIT CHANGERenal Systems, 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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