FDA 510(k)

AMER. V. MUELLER SURGICALSTAPLES-CARTR

K-Number: K833704 · 1983-12-29

Decision Date1983-12-29

Product CodeGDW

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

AMER. V. MUELLER SURGICALSTAPLES-CARTR is the device name listed in this FDA 510(k) record. The listed applicant is American Heyer Schulte. It received FDA 510(k) clearance on 1983-12-29 under 510(k) number K833704. The device is classified under product code GDW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMER. V. MUELLER SURGICALSTAPLES-CARTR?

AMER. V. MUELLER SURGICALSTAPLES-CARTR is a medical device that received FDA 510(k) clearance on 1983-12-29. The listed applicant is American Heyer Schulte. The 510(k) number is K833704.

When did AMER. V. MUELLER SURGICALSTAPLES-CARTR receive FDA 510(k) clearance?

AMER. V. MUELLER SURGICALSTAPLES-CARTR received FDA 510(k) clearance on 1983-12-29, under 510(k) number K833704.

Who is the listed applicant for AMER. V. MUELLER SURGICALSTAPLES-CARTR?

The FDA 510(k) record lists American Heyer Schulte as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AMER. V. MUELLER SURGICALSTAPLES-CARTR?

The FDA product code for AMER. V. MUELLER SURGICALSTAPLES-CARTR is GDW.

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Other records listing American Heyer Schulte as applicant

K840172VENTRAL WALL DEFECT REDUCT SILO K834593ONE-PIECE SHUNT K833502RADOVAN SUBCUTANEOUS TISSUE EXPANDER K833698AMER. V. MUELLER SURG. STAPLES ILA K832738HEYER-SCHULTE AFTERLOADING CATHETER K823790VENTRICULAR ACCESS SYSTEM

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Related Devices (Code: GDW)

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.