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FDA 510(k)

ULTRASOUND IMAGING SYSTEM MODEL 280 SL

K-Number: K860697 · 1986-07-24

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1986-07-24
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent for Some Indications

Device Summary

ULTRASOUND IMAGING SYSTEM MODEL 280 SL is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1986-07-24 under 510(k) number K860697. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the ULTRASOUND IMAGING SYSTEM MODEL 280 SL?

ULTRASOUND IMAGING SYSTEM MODEL 280 SL is a medical device that received FDA 510(k) clearance on 1986-07-24. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K860697.

When did ULTRASOUND IMAGING SYSTEM MODEL 280 SL receive FDA 510(k) clearance?

ULTRASOUND IMAGING SYSTEM MODEL 280 SL received FDA 510(k) clearance on 1986-07-24, under 510(k) number K860697.

Who is the listed applicant for ULTRASOUND IMAGING SYSTEM MODEL 280 SL?

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

What is the FDA product code for ULTRASOUND IMAGING SYSTEM MODEL 280 SL?

The FDA product code for ULTRASOUND IMAGING SYSTEM MODEL 280 SL is IYO.

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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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