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)

DIGITAL CUFF PV GAUGE

K-Number: K900755 · 1990-04-26

Decision Date1990-04-26
Product CodeBSK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DIGITAL CUFF PV GAUGE is the device name listed in this FDA 510(k) record. The listed applicant is International Medical Products, Inc.. It received FDA 510(k) clearance on 1990-04-26 under 510(k) number K900755. The device is classified under product code BSK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGITAL CUFF PV GAUGE?

DIGITAL CUFF PV GAUGE is a medical device that received FDA 510(k) clearance on 1990-04-26. The listed applicant is International Medical Products, Inc.. The 510(k) number is K900755.

When did DIGITAL CUFF PV GAUGE receive FDA 510(k) clearance?

DIGITAL CUFF PV GAUGE received FDA 510(k) clearance on 1990-04-26, under 510(k) number K900755.

Who is the listed applicant for DIGITAL CUFF PV GAUGE?

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

What is the FDA product code for DIGITAL CUFF PV GAUGE?

The FDA product code for DIGITAL CUFF PV GAUGE is BSK.

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 International Medical 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 9 devices →

Related Devices (Code: BSK)

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.

↑