KARL STORZ TAKE-APART(R) SUTURE FORCEPS, KARL STORZ KNOT TIER
K-Number: K945890 · 1995-02-17
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Device Summary
Frequently Asked Questions
What is the KARL STORZ TAKE-APART(R) SUTURE FORCEPS, KARL STORZ KNOT TIER?
KARL STORZ TAKE-APART(R) SUTURE FORCEPS, KARL STORZ KNOT TIER is a medical device that received FDA 510(k) clearance on 1995-02-17. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K945890.
When did KARL STORZ TAKE-APART(R) SUTURE FORCEPS, KARL STORZ KNOT TIER receive FDA 510(k) clearance?
KARL STORZ TAKE-APART(R) SUTURE FORCEPS, KARL STORZ KNOT TIER received FDA 510(k) clearance on 1995-02-17, under 510(k) number K945890.
Who is the listed applicant for KARL STORZ TAKE-APART(R) SUTURE FORCEPS, KARL STORZ KNOT TIER?
The FDA 510(k) record lists KARL STORZ Endoscopy-America, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for KARL STORZ TAKE-APART(R) SUTURE FORCEPS, KARL STORZ KNOT TIER?
The FDA product code for KARL STORZ TAKE-APART(R) SUTURE FORCEPS, KARL STORZ KNOT TIER is GCJ.
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 KARL STORZ Endoscopy-America, Inc. 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: GCJ)
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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