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FDA 510(k)

BASAL MEDIUM EAGLE W/EARLES SALTS, &

K-Number: K831745 · 1983-07-06

Decision Date1983-07-06
Product CodeKIT
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

BASAL MEDIUM EAGLE W/EARLES SALTS, & is the device name listed in this FDA 510(k) record. The listed applicant is Sigma Chemical Co.. It received FDA 510(k) clearance on 1983-07-06 under 510(k) number K831745. The device is classified under product code KIT. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BASAL MEDIUM EAGLE W/EARLES SALTS, &?

BASAL MEDIUM EAGLE W/EARLES SALTS, & is a medical device that received FDA 510(k) clearance on 1983-07-06. The listed applicant is Sigma Chemical Co.. The 510(k) number is K831745.

When did BASAL MEDIUM EAGLE W/EARLES SALTS, & receive FDA 510(k) clearance?

BASAL MEDIUM EAGLE W/EARLES SALTS, & received FDA 510(k) clearance on 1983-07-06, under 510(k) number K831745.

Who is the listed applicant for BASAL MEDIUM EAGLE W/EARLES SALTS, &?

The FDA 510(k) record lists Sigma Chemical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BASAL MEDIUM EAGLE W/EARLES SALTS, &?

The FDA product code for BASAL MEDIUM EAGLE W/EARLES SALTS, & is KIT.

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 Sigma Chemical 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 231 devices →

Related Devices (Code: KIT)

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

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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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