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FDA 510(k)

PULSE RF TEST

K-Number: K923771 · 1992-10-05

ApplicantPulse Scientific, Inc.
Decision Date1992-10-05
Product CodeDHR
Advisory CommitteeIM
DecisionSubstantially Equivalent

Device Summary

PULSE RF TEST is the device name listed in this FDA 510(k) record. The listed applicant is Pulse Scientific, Inc.. It received FDA 510(k) clearance on 1992-10-05 under 510(k) number K923771. The device is classified under product code DHR. It was reviewed by the IM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PULSE RF TEST?

PULSE RF TEST is a medical device that received FDA 510(k) clearance on 1992-10-05. The listed applicant is Pulse Scientific, Inc.. The 510(k) number is K923771.

When did PULSE RF TEST receive FDA 510(k) clearance?

PULSE RF TEST received FDA 510(k) clearance on 1992-10-05, under 510(k) number K923771.

Who is the listed applicant for PULSE RF TEST?

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

What is the FDA product code for PULSE RF TEST?

The FDA product code for PULSE RF TEST is DHR.

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.

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Other records listing Pulse Scientific, 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.

K923768PULSE CRP TESTK923767PULSE IM RED CELL TEST

Related Devices (Code: DHR)

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.

K192727K-ASSAY (R) RF (Ver.2), K-ASSAY (R) RF Calibrator (Ver.2)Kamiya Biomedical CompanyK190088QUANTA Flash RF IgM Reagents, QUANTA Flash RF IgA ReagentsInova Diagnostics, Inc.K182747EliA RF IgM ImmunoassayPhadia ABK162263Optilite Rheumatoid Factor KitThe Binding Site Group , Ltd.K160070Rheumatoid Factor (RF) Kit for use on SPAPLUSThe Binding Site Group , Ltd.K102673RHEUMATOID FACTOR IMMUNOLOGICAL TEST SYSTEMPhadia US, Inc.

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.

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