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FDA 510(k)

HSC UNIT ROD

K-Number: K896603 · 1990-01-30

Decision Date1990-01-30
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

HSC UNIT ROD is the device name listed in this FDA 510(k) record. The listed applicant is Danek Medical, Inc.. It received FDA 510(k) clearance on 1990-01-30 under 510(k) number K896603. The device is classified under product code KWP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HSC UNIT ROD?

HSC UNIT ROD is a medical device that received FDA 510(k) clearance on 1990-01-30. The listed applicant is Danek Medical, Inc.. The 510(k) number is K896603.

When did HSC UNIT ROD receive FDA 510(k) clearance?

HSC UNIT ROD received FDA 510(k) clearance on 1990-01-30, under 510(k) number K896603.

Who is the listed applicant for HSC UNIT ROD?

The FDA 510(k) record lists Danek Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HSC UNIT ROD?

The FDA product code for HSC UNIT ROD is KWP.

Other records listing Danek Medical, 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 56 devices →

Related Devices (Code: KWP)

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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