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FDA 510(k)

API TURBICITY STANDARD

K-Number: K810762 · 1981-04-03

ApplicantAnalytical Products, Inc.
Decision Date1981-04-03
Product CodeJKP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

API TURBICITY STANDARD 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 1981-04-03 under 510(k) number K810762. The device is classified under product code JKP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the API TURBICITY STANDARD?

API TURBICITY STANDARD is a medical device that received FDA 510(k) clearance on 1981-04-03. The listed applicant is Analytical Products, Inc.. The 510(k) number is K810762.

When did API TURBICITY STANDARD receive FDA 510(k) clearance?

API TURBICITY STANDARD received FDA 510(k) clearance on 1981-04-03, under 510(k) number K810762.

Who is the listed applicant for API TURBICITY STANDARD?

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 TURBICITY STANDARD?

The FDA product code for API TURBICITY STANDARD is JKP.

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Other records listing Analytical Products, 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.

K924814API 20E/UNISCEPT 20EK923684API UNISCEPT MIC/TYPE 2 AND 3 AND MICRO MICK922926API UNISCEPT KB/TYPE 2 AND 3K901559MODIFICATION TO API UNISCEPT 20GPK901390DMAC INDOLE REAGENTK895796API UNISCEPT KB

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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