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FDA 510(k)

GAS SAMPLING LINES AND CONNECTORS

K-Number: K932710 · 1993-07-23

Decision Date1993-07-23
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

GAS SAMPLING LINES AND CONNECTORS is the device name listed in this FDA 510(k) record. The listed applicant is Precision Med Products, Ltd.. It received FDA 510(k) clearance on 1993-07-23 under 510(k) number K932710. The device is classified under product code CAI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GAS SAMPLING LINES AND CONNECTORS?

GAS SAMPLING LINES AND CONNECTORS is a medical device that received FDA 510(k) clearance on 1993-07-23. The listed applicant is Precision Med Products, Ltd.. The 510(k) number is K932710.

When did GAS SAMPLING LINES AND CONNECTORS receive FDA 510(k) clearance?

GAS SAMPLING LINES AND CONNECTORS received FDA 510(k) clearance on 1993-07-23, under 510(k) number K932710.

Who is the listed applicant for GAS SAMPLING LINES AND CONNECTORS?

The FDA 510(k) record lists Precision Med Products, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for GAS SAMPLING LINES AND CONNECTORS?

The FDA product code for GAS SAMPLING LINES AND CONNECTORS is CAI.

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 Precision Med Products, Ltd. 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 16 devices →

Related Devices (Code: CAI)

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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