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FDA 510(k)

SUSPENSION SALINE, API 20E

K-Number: K770926 · 1977-06-17

ApplicantAnalytical Products, Inc.
Decision Date1977-06-17
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SUSPENSION SALINE, API 20E 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 1977-06-17 under 510(k) number K770926. The device is classified under product code JTO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUSPENSION SALINE, API 20E?

SUSPENSION SALINE, API 20E is a medical device that received FDA 510(k) clearance on 1977-06-17. The listed applicant is Analytical Products, Inc.. The 510(k) number is K770926.

When did SUSPENSION SALINE, API 20E receive FDA 510(k) clearance?

SUSPENSION SALINE, API 20E received FDA 510(k) clearance on 1977-06-17, under 510(k) number K770926.

Who is the listed applicant for SUSPENSION SALINE, API 20E?

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 SUSPENSION SALINE, API 20E?

The FDA product code for SUSPENSION SALINE, API 20E is JTO.

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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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Related Devices (Code: JTO)

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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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