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FDA 510(k)

TECHNICON SMA & AAII SYSTEMS

K-Number: K770406 · 1977-06-02

Decision Date1977-06-02
Product CodeCJE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

TECHNICON SMA & AAII SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Boehringer Laboratories. It received FDA 510(k) clearance on 1977-06-02 under 510(k) number K770406. The device is classified under product code CJE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TECHNICON SMA & AAII SYSTEMS?

TECHNICON SMA & AAII SYSTEMS is a medical device that received FDA 510(k) clearance on 1977-06-02. The listed applicant is Boehringer Laboratories. The 510(k) number is K770406.

When did TECHNICON SMA & AAII SYSTEMS receive FDA 510(k) clearance?

TECHNICON SMA & AAII SYSTEMS received FDA 510(k) clearance on 1977-06-02, under 510(k) number K770406.

Who is the listed applicant for TECHNICON SMA & AAII SYSTEMS?

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

What is the FDA product code for TECHNICON SMA & AAII SYSTEMS?

The FDA product code for TECHNICON SMA & AAII SYSTEMS is CJE.

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 Boehringer Laboratories 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 38 devices →

Related Devices (Code: CJE)

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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