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FDA 510(k)

MODEL 102 PH METER

K-Number: K870811 · 1987-03-24

ApplicantMesa Medical, Inc.
Decision Date1987-03-24
Product CodeLRI
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODEL 102 PH 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 1987-03-24 under 510(k) number K870811. The device is classified under product code LRI. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 102 PH METER?

MODEL 102 PH METER is a medical device that received FDA 510(k) clearance on 1987-03-24. The listed applicant is Mesa Medical, Inc.. The 510(k) number is K870811.

When did MODEL 102 PH METER receive FDA 510(k) clearance?

MODEL 102 PH METER received FDA 510(k) clearance on 1987-03-24, under 510(k) number K870811.

Who is the listed applicant for MODEL 102 PH 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 102 PH METER?

The FDA product code for MODEL 102 PH METER is LRI.

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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, MODIFICATIONK882032MODEL 90DX MULTITEST METERK852749RECOMMENDED ALTERNATIVE DIALYZER DISINFECTANTK843520WAREXIN RECOMMENDED ALTERNATIVE DIALYZK834447ECHO MM1000K821383ECHO, MODEL MM-1000

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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.

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