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FDA 510(k)

KARL STORZ TAKE-APART(R) SUTURE FORCEPS, KNOT TIER

K-Number: K945982 · 1995-03-21

Decision Date1995-03-21
Product CodeHET
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

KARL STORZ TAKE-APART(R) SUTURE FORCEPS, KNOT TIER is the device name listed in this FDA 510(k) record. The listed applicant is KARL STORZ Endoscopy-America, Inc.. It received FDA 510(k) clearance on 1995-03-21 under 510(k) number K945982. The device is classified under product code HET. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KARL STORZ TAKE-APART(R) SUTURE FORCEPS, KNOT TIER?

KARL STORZ TAKE-APART(R) SUTURE FORCEPS, KNOT TIER is a medical device that received FDA 510(k) clearance on 1995-03-21. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K945982.

When did KARL STORZ TAKE-APART(R) SUTURE FORCEPS, KNOT TIER receive FDA 510(k) clearance?

KARL STORZ TAKE-APART(R) SUTURE FORCEPS, KNOT TIER received FDA 510(k) clearance on 1995-03-21, under 510(k) number K945982.

Who is the listed applicant for KARL STORZ TAKE-APART(R) SUTURE FORCEPS, 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, KNOT TIER?

The FDA product code for KARL STORZ TAKE-APART(R) SUTURE FORCEPS, KNOT TIER is HET.

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.

View all 355 devices →

Related Devices (Code: HET)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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