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FDA 510(k)

API MDS*

K-Number: K823785 · 1983-01-09

ApplicantAnalytical Products, Inc.
Decision Date1983-01-09
Product CodeJQP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

API MDS* is the device name listed in this FDA 510(k) record. The listed applicant is Analytical Products, Inc.. It received FDA 510(k) clearance on 1983-01-09 under 510(k) number K823785. The device is classified under product code JQP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the API MDS*?

API MDS* is a medical device that received FDA 510(k) clearance on 1983-01-09. The listed applicant is Analytical Products, Inc.. The 510(k) number is K823785.

When did API MDS* receive FDA 510(k) clearance?

API MDS* received FDA 510(k) clearance on 1983-01-09, under 510(k) number K823785.

Who is the listed applicant for API MDS*?

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

What is the FDA product code for API MDS*?

The FDA product code for API MDS* is JQP.

Other records listing Analytical Products, Inc. as applicant

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Related Devices (Code: JQP)

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.

K113007BIONIME DIABETES MANAGEMENT SYSTEM VI.0Bionime CorporationK983468FASTTAKE ADAPTER, MODEL # P/N 020-072-01Selfcare, Inc.K964460THE ROBOLITEShai Syg Motion and Innovations, Ltd.K953652PRENVAL IBase Ten Systems, Inc.K934111MR7000 WITH TIME MANAGER SOFTWARE (TMS)Dynatech Laboratories, Inc.K923316EXPRESSO CARTRIDGEBio-Rad Laboratories, 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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