BACKHAUS CLAMP, 5 1/4
K-Number: K821293 · 1982-05-28
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Device Summary
Frequently Asked Questions
What is the BACKHAUS CLAMP, 5 1/4?
BACKHAUS CLAMP, 5 1/4 is a medical device that received FDA 510(k) clearance on 1982-05-28. The listed applicant is Conphar, Inc.. The 510(k) number is K821293.
When did BACKHAUS CLAMP, 5 1/4 receive FDA 510(k) clearance?
BACKHAUS CLAMP, 5 1/4 received FDA 510(k) clearance on 1982-05-28, under 510(k) number K821293.
Who is the listed applicant for BACKHAUS CLAMP, 5 1/4?
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 BACKHAUS CLAMP, 5 1/4?
The FDA product code for BACKHAUS CLAMP, 5 1/4 is HTD.
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: HTD)
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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