Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

GAS SAMPLING KIT MODIFICATION

K-Number: K921510 · 1992-06-11

Decision Date1992-06-11
Product CodeBZO
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

GAS SAMPLING KIT MODIFICATION is the device name listed in this FDA 510(k) record. The listed applicant is Respiratory Support Products, Inc.. It received FDA 510(k) clearance on 1992-06-11 under 510(k) number K921510. The device is classified under product code BZO. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GAS SAMPLING KIT MODIFICATION?

GAS SAMPLING KIT MODIFICATION is a medical device that received FDA 510(k) clearance on 1992-06-11. The listed applicant is Respiratory Support Products, Inc.. The 510(k) number is K921510.

When did GAS SAMPLING KIT MODIFICATION receive FDA 510(k) clearance?

GAS SAMPLING KIT MODIFICATION received FDA 510(k) clearance on 1992-06-11, under 510(k) number K921510.

Who is the listed applicant for GAS SAMPLING KIT MODIFICATION?

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

What is the FDA product code for GAS SAMPLING KIT MODIFICATION?

The FDA product code for GAS SAMPLING KIT MODIFICATION is BZO.

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 Respiratory Support Products, 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.

View all 27 devices →

Related Devices (Code: BZO)

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.

↑