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FDA 510(k)

SHEPARD LENS FORCEP W/ IRRIGA W/OUT LOCK

K-Number: K770099 · 1977-01-24

Decision Date1977-01-24
Product CodeHNR
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SHEPARD LENS FORCEP W/ IRRIGA W/OUT LOCK is the device name listed in this FDA 510(k) record. The listed applicant is Edward Weck, Inc.. It received FDA 510(k) clearance on 1977-01-24 under 510(k) number K770099. The device is classified under product code HNR. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SHEPARD LENS FORCEP W/ IRRIGA W/OUT LOCK?

SHEPARD LENS FORCEP W/ IRRIGA W/OUT LOCK is a medical device that received FDA 510(k) clearance on 1977-01-24. The listed applicant is Edward Weck, Inc.. The 510(k) number is K770099.

When did SHEPARD LENS FORCEP W/ IRRIGA W/OUT LOCK receive FDA 510(k) clearance?

SHEPARD LENS FORCEP W/ IRRIGA W/OUT LOCK received FDA 510(k) clearance on 1977-01-24, under 510(k) number K770099.

Who is the listed applicant for SHEPARD LENS FORCEP W/ IRRIGA W/OUT 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 LENS FORCEP W/ IRRIGA W/OUT LOCK?

The FDA product code for SHEPARD LENS FORCEP W/ IRRIGA W/OUT 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.

View all 140 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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