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FDA 510(k)

BSI MODEL MCT 7000-THERMAL IMAGING SYSTEM

K-Number: K850534 · 1985-02-27

ApplicantBales Scientific, Inc.
Decision Date1985-02-27
Product CodeLHQ
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

BSI MODEL MCT 7000-THERMAL IMAGING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Bales Scientific, Inc.. It received FDA 510(k) clearance on 1985-02-27 under 510(k) number K850534. The device is classified under product code LHQ. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BSI MODEL MCT 7000-THERMAL IMAGING SYSTEM?

BSI MODEL MCT 7000-THERMAL IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 1985-02-27. The listed applicant is Bales Scientific, Inc.. The 510(k) number is K850534.

When did BSI MODEL MCT 7000-THERMAL IMAGING SYSTEM receive FDA 510(k) clearance?

BSI MODEL MCT 7000-THERMAL IMAGING SYSTEM received FDA 510(k) clearance on 1985-02-27, under 510(k) number K850534.

Who is the listed applicant for BSI MODEL MCT 7000-THERMAL IMAGING SYSTEM?

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

What is the FDA product code for BSI MODEL MCT 7000-THERMAL IMAGING SYSTEM?

The FDA product code for BSI MODEL MCT 7000-THERMAL IMAGING SYSTEM is LHQ.

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.

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Other records listing Bales Scientific, 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.

K974468PHOTONIC STIMULATORK897191BSI MODEL TIP

Related Devices (Code: LHQ)

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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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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