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FDA 510(k)

HYPERTHERMIA SENSOR ACCESSORIES

K-Number: K900048 · 1990-07-02

ApplicantValley Medical Research, Inc.
Decision Date1990-07-02
Product CodeFLL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HYPERTHERMIA SENSOR ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Valley Medical Research, Inc.. It received FDA 510(k) clearance on 1990-07-02 under 510(k) number K900048. The device is classified under product code FLL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HYPERTHERMIA SENSOR ACCESSORIES?

HYPERTHERMIA SENSOR ACCESSORIES is a medical device that received FDA 510(k) clearance on 1990-07-02. The listed applicant is Valley Medical Research, Inc.. The 510(k) number is K900048.

When did HYPERTHERMIA SENSOR ACCESSORIES receive FDA 510(k) clearance?

HYPERTHERMIA SENSOR ACCESSORIES received FDA 510(k) clearance on 1990-07-02, under 510(k) number K900048.

Who is the listed applicant for HYPERTHERMIA SENSOR ACCESSORIES?

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

What is the FDA product code for HYPERTHERMIA SENSOR ACCESSORIES?

The FDA product code for HYPERTHERMIA SENSOR ACCESSORIES is FLL.

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Related Devices (Code: FLL)

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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Official Source

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