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FDA 510(k)

90DX MULTITEST METER, MODIFICATION

K-Number: K925210 · 1994-01-25

ApplicantMesa Medical, Inc.
Decision Date1994-01-25
Product CodeFLB
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

90DX MULTITEST METER, MODIFICATION 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 1994-01-25 under 510(k) number K925210. 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 90DX MULTITEST METER, MODIFICATION?

90DX MULTITEST METER, MODIFICATION is a medical device that received FDA 510(k) clearance on 1994-01-25. The listed applicant is Mesa Medical, Inc.. The 510(k) number is K925210.

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

90DX MULTITEST METER, MODIFICATION received FDA 510(k) clearance on 1994-01-25, under 510(k) number K925210.

Who is the listed applicant for 90DX MULTITEST METER, MODIFICATION?

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 90DX MULTITEST METER, MODIFICATION?

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

Related Clinical Trials

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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.

K882032MODEL 90DX MULTITEST METERK870811MODEL 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 CompanyK882032MODEL 90DX MULTITEST METERMesa 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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