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)

KELLER VITAL SIGNS MONITOR - KMS-890

K-Number: K910262 · 1991-04-01

Decision Date1991-04-01
Product CodeDSJ
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

KELLER VITAL SIGNS MONITOR - KMS-890 is the device name listed in this FDA 510(k) record. The listed applicant is Keller Medical Specialties Products, Inc.. It received FDA 510(k) clearance on 1991-04-01 under 510(k) number K910262. The device is classified under product code DSJ. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KELLER VITAL SIGNS MONITOR - KMS-890?

KELLER VITAL SIGNS MONITOR - KMS-890 is a medical device that received FDA 510(k) clearance on 1991-04-01. The listed applicant is Keller Medical Specialties Products, Inc.. The 510(k) number is K910262.

When did KELLER VITAL SIGNS MONITOR - KMS-890 receive FDA 510(k) clearance?

KELLER VITAL SIGNS MONITOR - KMS-890 received FDA 510(k) clearance on 1991-04-01, under 510(k) number K910262.

Who is the listed applicant for KELLER VITAL SIGNS MONITOR - KMS-890?

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

What is the FDA product code for KELLER VITAL SIGNS MONITOR - KMS-890?

The FDA product code for KELLER VITAL SIGNS MONITOR - KMS-890 is DSJ.

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 Keller Medical Specialties 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.

Related Devices (Code: DSJ)

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.

↑