DODICK LENS HOLDING FORCEPS
K-Number: K801467 · 1980-07-28
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Device Summary
Frequently Asked Questions
What is the DODICK LENS HOLDING FORCEPS?
DODICK LENS HOLDING FORCEPS is a medical device that received FDA 510(k) clearance on 1980-07-28. The listed applicant is Edward Weck, Inc.. The 510(k) number is K801467.
When did DODICK LENS HOLDING FORCEPS receive FDA 510(k) clearance?
DODICK LENS HOLDING FORCEPS received FDA 510(k) clearance on 1980-07-28, under 510(k) number K801467.
Who is the listed applicant for DODICK LENS HOLDING FORCEPS?
The FDA 510(k) record lists Edward Weck, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DODICK LENS HOLDING FORCEPS?
The FDA product code for DODICK LENS HOLDING FORCEPS is HNR.
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 Edward 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: HNR)
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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