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FDA 510(k)

THORACIC GAUGE #TG-60 -VACUUM REGULATOR

K-Number: K831505 · 1983-07-12

ApplicantSorensen Research
Decision Date1983-07-12
Product CodeKDP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

THORACIC GAUGE #TG-60 -VACUUM REGULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Sorensen Research. It received FDA 510(k) clearance on 1983-07-12 under 510(k) number K831505. The device is classified under product code KDP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THORACIC GAUGE #TG-60 -VACUUM REGULATOR?

THORACIC GAUGE #TG-60 -VACUUM REGULATOR is a medical device that received FDA 510(k) clearance on 1983-07-12. The listed applicant is Sorensen Research. The 510(k) number is K831505.

When did THORACIC GAUGE #TG-60 -VACUUM REGULATOR receive FDA 510(k) clearance?

THORACIC GAUGE #TG-60 -VACUUM REGULATOR received FDA 510(k) clearance on 1983-07-12, under 510(k) number K831505.

Who is the listed applicant for THORACIC GAUGE #TG-60 -VACUUM REGULATOR?

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

What is the FDA product code for THORACIC GAUGE #TG-60 -VACUUM REGULATOR?

The FDA product code for THORACIC GAUGE #TG-60 -VACUUM REGULATOR is KDP.

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Other records listing Sorensen Research as applicant

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Related Devices (Code: KDP)

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

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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