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FDA 510(k)

SCANO 731B & 731C ULTRASOUND SOFT TIS DEPT MEAS SY

K-Number: K853147 · 1986-03-13

ApplicantScano, Inc.
Decision Date1986-03-13
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

SCANO 731B & 731C ULTRASOUND SOFT TIS DEPT MEAS SY is the device name listed in this FDA 510(k) record. The listed applicant is Scano, Inc.. It received FDA 510(k) clearance on 1986-03-13 under 510(k) number K853147. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCANO 731B & 731C ULTRASOUND SOFT TIS DEPT MEAS SY?

SCANO 731B & 731C ULTRASOUND SOFT TIS DEPT MEAS SY is a medical device that received FDA 510(k) clearance on 1986-03-13. The listed applicant is Scano, Inc.. The 510(k) number is K853147.

When did SCANO 731B & 731C ULTRASOUND SOFT TIS DEPT MEAS SY receive FDA 510(k) clearance?

SCANO 731B & 731C ULTRASOUND SOFT TIS DEPT MEAS SY received FDA 510(k) clearance on 1986-03-13, under 510(k) number K853147.

Who is the listed applicant for SCANO 731B & 731C ULTRASOUND SOFT TIS DEPT MEAS SY?

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

What is the FDA product code for SCANO 731B & 731C ULTRASOUND SOFT TIS DEPT MEAS SY?

The FDA product code for SCANO 731B & 731C ULTRASOUND SOFT TIS DEPT MEAS SY 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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