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)

CPR MICROMASK WITH OXYGEN INLET

K-Number: K953414 · 1996-03-20

ApplicantPlasco, Inc.
Decision Date1996-03-20
Product CodeCBP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CPR MICROMASK WITH OXYGEN INLET is the device name listed in this FDA 510(k) record. The listed applicant is Plasco, Inc.. It received FDA 510(k) clearance on 1996-03-20 under 510(k) number K953414. The device is classified under product code CBP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CPR MICROMASK WITH OXYGEN INLET?

CPR MICROMASK WITH OXYGEN INLET is a medical device that received FDA 510(k) clearance on 1996-03-20. The listed applicant is Plasco, Inc.. The 510(k) number is K953414.

When did CPR MICROMASK WITH OXYGEN INLET receive FDA 510(k) clearance?

CPR MICROMASK WITH OXYGEN INLET received FDA 510(k) clearance on 1996-03-20, under 510(k) number K953414.

Who is the listed applicant for CPR MICROMASK WITH OXYGEN INLET?

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

What is the FDA product code for CPR MICROMASK WITH OXYGEN INLET?

The FDA product code for CPR MICROMASK WITH OXYGEN INLET is CBP.

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 Plasco, 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 16 devices →

Related Devices (Code: CBP)

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.

↑