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FDA 510(k)

FISCHER/KRYSTAL THERAPEUTIC ULTRASOUND

K-Number: K861837 · 1986-08-07

Decision Date1986-08-07
Product CodeIMG
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

FISCHER/KRYSTAL THERAPEUTIC ULTRASOUND is the device name listed in this FDA 510(k) record. The listed applicant is Fischer Industries, Inc.. It received FDA 510(k) clearance on 1986-08-07 under 510(k) number K861837. The device is classified under product code IMG. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FISCHER/KRYSTAL THERAPEUTIC ULTRASOUND?

FISCHER/KRYSTAL THERAPEUTIC ULTRASOUND is a medical device that received FDA 510(k) clearance on 1986-08-07. The listed applicant is Fischer Industries, Inc.. The 510(k) number is K861837.

When did FISCHER/KRYSTAL THERAPEUTIC ULTRASOUND receive FDA 510(k) clearance?

FISCHER/KRYSTAL THERAPEUTIC ULTRASOUND received FDA 510(k) clearance on 1986-08-07, under 510(k) number K861837.

Who is the listed applicant for FISCHER/KRYSTAL THERAPEUTIC ULTRASOUND?

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

What is the FDA product code for FISCHER/KRYSTAL THERAPEUTIC ULTRASOUND?

The FDA product code for FISCHER/KRYSTAL THERAPEUTIC ULTRASOUND is IMG.

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 Fischer Industries, 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: IMG)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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