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FDA 510(k)

INTEROPERATIVE LINEAR/SECTOR ULTRASOUND SCANNER

K-Number: K855247 · 1987-02-19

ApplicantCodman & Shurtleff, Inc.
Decision Date1987-02-19
Product CodeITX
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

INTEROPERATIVE LINEAR/SECTOR ULTRASOUND SCANNER is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 1987-02-19 under 510(k) number K855247. The device is classified under product code ITX. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTEROPERATIVE LINEAR/SECTOR ULTRASOUND SCANNER?

INTEROPERATIVE LINEAR/SECTOR ULTRASOUND SCANNER is a medical device that received FDA 510(k) clearance on 1987-02-19. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K855247.

When did INTEROPERATIVE LINEAR/SECTOR ULTRASOUND SCANNER receive FDA 510(k) clearance?

INTEROPERATIVE LINEAR/SECTOR ULTRASOUND SCANNER received FDA 510(k) clearance on 1987-02-19, under 510(k) number K855247.

Who is the listed applicant for INTEROPERATIVE LINEAR/SECTOR ULTRASOUND SCANNER?

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

What is the FDA product code for INTEROPERATIVE LINEAR/SECTOR ULTRASOUND SCANNER?

The FDA product code for INTEROPERATIVE LINEAR/SECTOR ULTRASOUND SCANNER is ITX.

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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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