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FDA 510(k)

CKS OSCILLATING SAW BLADE

K-Number: K921131 · 1992-06-08

Decision Date1992-06-08
Product CodeHWE
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CKS OSCILLATING SAW BLADE is the device name listed in this FDA 510(k) record. The listed applicant is Techmedica, Inc.. It received FDA 510(k) clearance on 1992-06-08 under 510(k) number K921131. The device is classified under product code HWE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CKS OSCILLATING SAW BLADE?

CKS OSCILLATING SAW BLADE is a medical device that received FDA 510(k) clearance on 1992-06-08. The listed applicant is Techmedica, Inc.. The 510(k) number is K921131.

When did CKS OSCILLATING SAW BLADE receive FDA 510(k) clearance?

CKS OSCILLATING SAW BLADE received FDA 510(k) clearance on 1992-06-08, under 510(k) number K921131.

Who is the listed applicant for CKS OSCILLATING SAW BLADE?

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

What is the FDA product code for CKS OSCILLATING SAW BLADE?

The FDA product code for CKS OSCILLATING SAW BLADE is HWE.

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 Techmedica, 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 31 devices →

Related Devices (Code: HWE)

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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