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)

STAT BLUE DISPOS. MANUAL RESUSCITATOR

K-Number: K850436 · 1985-02-26

Decision Date1985-02-26
Product CodeBTM
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

STAT BLUE DISPOS. MANUAL RESUSCITATOR is the device name listed in this FDA 510(k) record. The listed applicant is Vital Signs, Inc.. It received FDA 510(k) clearance on 1985-02-26 under 510(k) number K850436. The device is classified under product code BTM. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STAT BLUE DISPOS. MANUAL RESUSCITATOR?

STAT BLUE DISPOS. MANUAL RESUSCITATOR is a medical device that received FDA 510(k) clearance on 1985-02-26. The listed applicant is Vital Signs, Inc.. The 510(k) number is K850436.

When did STAT BLUE DISPOS. MANUAL RESUSCITATOR receive FDA 510(k) clearance?

STAT BLUE DISPOS. MANUAL RESUSCITATOR received FDA 510(k) clearance on 1985-02-26, under 510(k) number K850436.

Who is the listed applicant for STAT BLUE DISPOS. MANUAL RESUSCITATOR?

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

What is the FDA product code for STAT BLUE DISPOS. MANUAL RESUSCITATOR?

The FDA product code for STAT BLUE DISPOS. MANUAL RESUSCITATOR is BTM.

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 Vital Signs, 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 75 devices →

Related Devices (Code: BTM)

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.

↑