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FDA 510(k)

TEMP STERNUM SAW

K-Number: K801914 · 1980-10-23

ApplicantTemp Medical Products, Inc.
Decision Date1980-10-23
Product CodeDWI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TEMP STERNUM SAW is the device name listed in this FDA 510(k) record. The listed applicant is Temp Medical Products, Inc.. It received FDA 510(k) clearance on 1980-10-23 under 510(k) number K801914. The device is classified under product code DWI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TEMP STERNUM SAW?

TEMP STERNUM SAW is a medical device that received FDA 510(k) clearance on 1980-10-23. The listed applicant is Temp Medical Products, Inc.. The 510(k) number is K801914.

When did TEMP STERNUM SAW receive FDA 510(k) clearance?

TEMP STERNUM SAW received FDA 510(k) clearance on 1980-10-23, under 510(k) number K801914.

Who is the listed applicant for TEMP STERNUM SAW?

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

What is the FDA product code for TEMP STERNUM SAW?

The FDA product code for TEMP STERNUM SAW is DWI.

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.

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Other records listing Temp Medical Products, 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.

K830189CARDIOVASCULAR SAW BLADES

Related Devices (Code: DWI)

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.

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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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