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FDA 510(k)

LABELING FOR MYO/WIRE II STERNOTOMY SUTURES

K-Number: K932513 · 1994-01-07

ApplicantAlto Development Corp.
Decision Date1994-01-07
Product CodeGAO
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LABELING FOR MYO/WIRE II STERNOTOMY SUTURES is the device name listed in this FDA 510(k) record. The listed applicant is Alto Development Corp.. It received FDA 510(k) clearance on 1994-01-07 under 510(k) number K932513. The device is classified under product code GAO. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LABELING FOR MYO/WIRE II STERNOTOMY SUTURES?

LABELING FOR MYO/WIRE II STERNOTOMY SUTURES is a medical device that received FDA 510(k) clearance on 1994-01-07. The listed applicant is Alto Development Corp.. The 510(k) number is K932513.

When did LABELING FOR MYO/WIRE II STERNOTOMY SUTURES receive FDA 510(k) clearance?

LABELING FOR MYO/WIRE II STERNOTOMY SUTURES received FDA 510(k) clearance on 1994-01-07, under 510(k) number K932513.

Who is the listed applicant for LABELING FOR MYO/WIRE II STERNOTOMY SUTURES?

The FDA 510(k) record lists Alto Development Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LABELING FOR MYO/WIRE II STERNOTOMY SUTURES?

The FDA product code for LABELING FOR MYO/WIRE II STERNOTOMY SUTURES is GAO.

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Related Devices (Code: GAO)

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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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