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FDA 510(k)

API 3S

K-Number: K770176 · 1977-02-18

ApplicantAnalytical Products, Inc.
Decision Date1977-02-18
Product CodeJSE
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

API 3S 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 1977-02-18 under 510(k) number K770176. The device is classified under product code JSE. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the API 3S?

API 3S is a medical device that received FDA 510(k) clearance on 1977-02-18. The listed applicant is Analytical Products, Inc.. The 510(k) number is K770176.

When did API 3S receive FDA 510(k) clearance?

API 3S received FDA 510(k) clearance on 1977-02-18, under 510(k) number K770176.

Who is the listed applicant for API 3S?

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 3S?

The FDA product code for API 3S is JSE.

Other records listing Analytical Products, Inc. as applicant

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Related Devices (Code: JSE)

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.

K962265MLX MICROTITER PLATE LUMINOMETERDynatech Laboratories, Inc.K883995X-ACT UREA/TDAPro-Lab, Inc.K883996X-ACT LDC/INDPro-Lab, Inc.K880133MIL MEDIUMHardy MediaK880116MRVP BROTHHardy MediaK874537KLIGLER IRON AGAR AND TRIPLE SUGAR IRON AGARLakewood Biochemical Co., 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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