SHEPARD II, LENS FORCEP W/ LOCK
K-Number: K770105 · 1977-01-25
Advertisement
Device Summary
Frequently Asked Questions
What is the SHEPARD II, LENS FORCEP W/ LOCK?
SHEPARD II, LENS FORCEP W/ LOCK is a medical device that received FDA 510(k) clearance on 1977-01-25. The listed applicant is Edward Weck, Inc.. The 510(k) number is K770105.
When did SHEPARD II, LENS FORCEP W/ LOCK receive FDA 510(k) clearance?
SHEPARD II, LENS FORCEP W/ LOCK received FDA 510(k) clearance on 1977-01-25, under 510(k) number K770105.
Who is the listed applicant for SHEPARD II, LENS FORCEP W/ LOCK?
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 SHEPARD II, LENS FORCEP W/ LOCK?
The FDA product code for SHEPARD II, LENS FORCEP W/ LOCK 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.
Advertisement