PILLING WECK M-20 DISPOSABLE AUTOMATIC HEMOCLIP
K-Number: K944552 · 1994-11-07
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Device Summary
Frequently Asked Questions
What is the PILLING WECK M-20 DISPOSABLE AUTOMATIC HEMOCLIP?
PILLING WECK M-20 DISPOSABLE AUTOMATIC HEMOCLIP is a medical device that received FDA 510(k) clearance on 1994-11-07. The listed applicant is Pilling Weck, Inc.. The 510(k) number is K944552.
When did PILLING WECK M-20 DISPOSABLE AUTOMATIC HEMOCLIP receive FDA 510(k) clearance?
PILLING WECK M-20 DISPOSABLE AUTOMATIC HEMOCLIP received FDA 510(k) clearance on 1994-11-07, under 510(k) number K944552.
Who is the listed applicant for PILLING WECK M-20 DISPOSABLE AUTOMATIC HEMOCLIP?
The FDA 510(k) record lists Pilling Weck, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PILLING WECK M-20 DISPOSABLE AUTOMATIC HEMOCLIP?
The FDA product code for PILLING WECK M-20 DISPOSABLE AUTOMATIC HEMOCLIP is FZP.
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 Pilling Weck, 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: FZP)
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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