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FDA 510(k)

FELDMAN MINI-SAW, #300000

K-Number: K800669 · 1980-04-21

Decision Date1980-04-21
Product CodeEWQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

FELDMAN MINI-SAW, #300000 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 1980-04-21 under 510(k) number K800669. The device is classified under product code EWQ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FELDMAN MINI-SAW, #300000?

FELDMAN MINI-SAW, #300000 is a medical device that received FDA 510(k) clearance on 1980-04-21. The listed applicant is KARL STORZ Endoscopy-America, Inc.. The 510(k) number is K800669.

When did FELDMAN MINI-SAW, #300000 receive FDA 510(k) clearance?

FELDMAN MINI-SAW, #300000 received FDA 510(k) clearance on 1980-04-21, under 510(k) number K800669.

Who is the listed applicant for FELDMAN MINI-SAW, #300000?

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 FELDMAN MINI-SAW, #300000?

The FDA product code for FELDMAN MINI-SAW, #300000 is EWQ.

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: EWQ)

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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