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FDA 510(k)

SOLCO BASLE INTRAOPERATIVE AUTOTTRNSFUS

K-Number: K843821 · 1985-10-01

Decision Date1985-10-01
Product CodeCAC
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SOLCO BASLE INTRAOPERATIVE AUTOTTRNSFUS is the device name listed in this FDA 510(k) record. The listed applicant is Solco Basle, Inc.. It received FDA 510(k) clearance on 1985-10-01 under 510(k) number K843821. The device is classified under product code CAC. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SOLCO BASLE INTRAOPERATIVE AUTOTTRNSFUS?

SOLCO BASLE INTRAOPERATIVE AUTOTTRNSFUS is a medical device that received FDA 510(k) clearance on 1985-10-01. The listed applicant is Solco Basle, Inc.. The 510(k) number is K843821.

When did SOLCO BASLE INTRAOPERATIVE AUTOTTRNSFUS receive FDA 510(k) clearance?

SOLCO BASLE INTRAOPERATIVE AUTOTTRNSFUS received FDA 510(k) clearance on 1985-10-01, under 510(k) number K843821.

Who is the listed applicant for SOLCO BASLE INTRAOPERATIVE AUTOTTRNSFUS?

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

What is the FDA product code for SOLCO BASLE INTRAOPERATIVE AUTOTTRNSFUS?

The FDA product code for SOLCO BASLE INTRAOPERATIVE AUTOTTRNSFUS is CAC.

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 Solco Basle, 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.

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Related Devices (Code: CAC)

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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