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)

PROTECTAIDE CPR PROTECTION PACK NO. 17701

K-Number: K942466 · 1994-10-06

Decision Date1994-10-06
Product CodeCBP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PROTECTAIDE CPR PROTECTION PACK NO. 17701 is the device name listed in this FDA 510(k) record. The listed applicant is Protectaide, Inc.. It received FDA 510(k) clearance on 1994-10-06 under 510(k) number K942466. 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 PROTECTAIDE CPR PROTECTION PACK NO. 17701?

PROTECTAIDE CPR PROTECTION PACK NO. 17701 is a medical device that received FDA 510(k) clearance on 1994-10-06. The listed applicant is Protectaide, Inc.. The 510(k) number is K942466.

When did PROTECTAIDE CPR PROTECTION PACK NO. 17701 receive FDA 510(k) clearance?

PROTECTAIDE CPR PROTECTION PACK NO. 17701 received FDA 510(k) clearance on 1994-10-06, under 510(k) number K942466.

Who is the listed applicant for PROTECTAIDE CPR PROTECTION PACK NO. 17701?

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

What is the FDA product code for PROTECTAIDE CPR PROTECTION PACK NO. 17701?

The FDA product code for PROTECTAIDE CPR PROTECTION PACK NO. 17701 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 Protectaide, 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 11 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.

↑