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FDA 510(k)

4-9295 BARBITURATES TEST MIX

K-Number: K871174 · 1987-06-11

ApplicantSupelco, Inc.
Decision Date1987-06-11
Product CodeDKB
Advisory CommitteeTX
DecisionSubstantially Equivalent

Device Summary

4-9295 BARBITURATES TEST MIX is the device name listed in this FDA 510(k) record. The listed applicant is Supelco, Inc.. It received FDA 510(k) clearance on 1987-06-11 under 510(k) number K871174. The device is classified under product code DKB. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 4-9295 BARBITURATES TEST MIX?

4-9295 BARBITURATES TEST MIX is a medical device that received FDA 510(k) clearance on 1987-06-11. The listed applicant is Supelco, Inc.. The 510(k) number is K871174.

When did 4-9295 BARBITURATES TEST MIX receive FDA 510(k) clearance?

4-9295 BARBITURATES TEST MIX received FDA 510(k) clearance on 1987-06-11, under 510(k) number K871174.

Who is the listed applicant for 4-9295 BARBITURATES TEST MIX?

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

What is the FDA product code for 4-9295 BARBITURATES TEST MIX?

The FDA product code for 4-9295 BARBITURATES TEST MIX is DKB.

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 Supelco, 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.

View all 24 devices →

Related Devices (Code: DKB)

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.

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