CONPHAR PERCUSSION HAMMER(BUCK TYPE)
K-Number: K803174 · 1980-12-30
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Device Summary
Frequently Asked Questions
What is the CONPHAR PERCUSSION HAMMER(BUCK TYPE)?
CONPHAR PERCUSSION HAMMER(BUCK TYPE) is a medical device that received FDA 510(k) clearance on 1980-12-30. The listed applicant is Conphar, Inc.. The 510(k) number is K803174.
When did CONPHAR PERCUSSION HAMMER(BUCK TYPE) receive FDA 510(k) clearance?
CONPHAR PERCUSSION HAMMER(BUCK TYPE) received FDA 510(k) clearance on 1980-12-30, under 510(k) number K803174.
Who is the listed applicant for CONPHAR PERCUSSION HAMMER(BUCK TYPE)?
The FDA 510(k) record lists Conphar, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CONPHAR PERCUSSION HAMMER(BUCK TYPE)?
The FDA product code for CONPHAR PERCUSSION HAMMER(BUCK TYPE) is GWZ.
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 Conphar, 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.
Related Devices (Code: GWZ)
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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