AMER. V. MUELLER SURG. STAPLES ILA
K-Number: K833698 · 1984-01-25
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Device Summary
Frequently Asked Questions
What is the AMER. V. MUELLER SURG. STAPLES ILA?
AMER. V. MUELLER SURG. STAPLES ILA is a medical device that received FDA 510(k) clearance on 1984-01-25. The listed applicant is American Heyer Schulte. The 510(k) number is K833698.
When did AMER. V. MUELLER SURG. STAPLES ILA receive FDA 510(k) clearance?
AMER. V. MUELLER SURG. STAPLES ILA received FDA 510(k) clearance on 1984-01-25, under 510(k) number K833698.
Who is the listed applicant for AMER. V. MUELLER SURG. STAPLES ILA?
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 SURG. STAPLES ILA?
The FDA product code for AMER. V. MUELLER SURG. STAPLES ILA is GDW.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing American Heyer Schulte as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: GDW)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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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