Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ANALYTIX AUTO SAMPLE PREP. STA. 1600

K-Number: K770210 · 1977-02-14

Decision Date1977-02-14
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ANALYTIX AUTO SAMPLE PREP. STA. 1600 is the device name listed in this FDA 510(k) record. The listed applicant is G.D. Searle and Co.. It received FDA 510(k) clearance on 1977-02-14 under 510(k) number K770210. The device is classified under product code JQW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANALYTIX AUTO SAMPLE PREP. STA. 1600?

ANALYTIX AUTO SAMPLE PREP. STA. 1600 is a medical device that received FDA 510(k) clearance on 1977-02-14. The listed applicant is G.D. Searle and Co.. The 510(k) number is K770210.

When did ANALYTIX AUTO SAMPLE PREP. STA. 1600 receive FDA 510(k) clearance?

ANALYTIX AUTO SAMPLE PREP. STA. 1600 received FDA 510(k) clearance on 1977-02-14, under 510(k) number K770210.

Who is the listed applicant for ANALYTIX AUTO SAMPLE PREP. STA. 1600?

The FDA 510(k) record lists G.D. Searle and Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANALYTIX AUTO SAMPLE PREP. STA. 1600?

The FDA product code for ANALYTIX AUTO SAMPLE PREP. STA. 1600 is JQW.

Related Clinical Trials

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.

Other records listing G.D. Searle and Co. 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.

View all 56 devices →

Related Devices (Code: JQW)

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.

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.

↑