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FDA 510(k)

KARL STORZ TAKE-APART ROTATING GRASPING FORCEPS

K-Number: K952149 · 1995-06-15

ApplicantKARL STORZ Endoscopy-America, Inc.
Decision Date1995-06-15
Product CodeLQR
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

KARL STORZ TAKE-APART ROTATING GRASPING FORCEPS 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 1995-06-15 under 510(k) number K952149. The device is classified under product code LQR. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KARL STORZ TAKE-APART ROTATING GRASPING FORCEPS?

KARL STORZ TAKE-APART ROTATING GRASPING FORCEPS is a medical device that received FDA 510(k) clearance on 1995-06-15. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K952149.

When did KARL STORZ TAKE-APART ROTATING GRASPING FORCEPS receive FDA 510(k) clearance?

KARL STORZ TAKE-APART ROTATING GRASPING FORCEPS received FDA 510(k) clearance on 1995-06-15, under 510(k) number K952149.

Who is the listed applicant for KARL STORZ TAKE-APART ROTATING GRASPING FORCEPS?

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 ROTATING GRASPING FORCEPS?

The FDA product code for KARL STORZ TAKE-APART ROTATING GRASPING FORCEPS is LQR.

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Other records listing KARL STORZ Endoscopy-America, Inc. as applicant

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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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