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FDA 510(k)

KARL STORZ MODEL 28184 PNEUMATIC SHUTTLE SHAVER

K-Number: K871891 · 1987-06-05

Decision Date1987-06-05
Product CodeHSZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KARL STORZ MODEL 28184 PNEUMATIC SHUTTLE SHAVER 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 1987-06-05 under 510(k) number K871891. The device is classified under product code HSZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KARL STORZ MODEL 28184 PNEUMATIC SHUTTLE SHAVER?

KARL STORZ MODEL 28184 PNEUMATIC SHUTTLE SHAVER is a medical device that received FDA 510(k) clearance on 1987-06-05. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K871891.

When did KARL STORZ MODEL 28184 PNEUMATIC SHUTTLE SHAVER receive FDA 510(k) clearance?

KARL STORZ MODEL 28184 PNEUMATIC SHUTTLE SHAVER received FDA 510(k) clearance on 1987-06-05, under 510(k) number K871891.

Who is the listed applicant for KARL STORZ MODEL 28184 PNEUMATIC SHUTTLE SHAVER?

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 MODEL 28184 PNEUMATIC SHUTTLE SHAVER?

The FDA product code for KARL STORZ MODEL 28184 PNEUMATIC SHUTTLE SHAVER is HSZ.

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: HSZ)

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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