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FDA 510(k)

REPL. PISTON FOR TROUTMAN CORNEAL PUNCH

K-Number: K791988 · 1979-10-30

Decision Date1979-10-30
Product CodeHNJ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

REPL. PISTON FOR TROUTMAN CORNEAL PUNCH 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 1979-10-30 under 510(k) number K791988. The device is classified under product code HNJ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPL. PISTON FOR TROUTMAN CORNEAL PUNCH?

REPL. PISTON FOR TROUTMAN CORNEAL PUNCH is a medical device that received FDA 510(k) clearance on 1979-10-30. The listed applicant is Edward Weck, Inc.. The 510(k) number is K791988.

When did REPL. PISTON FOR TROUTMAN CORNEAL PUNCH receive FDA 510(k) clearance?

REPL. PISTON FOR TROUTMAN CORNEAL PUNCH received FDA 510(k) clearance on 1979-10-30, under 510(k) number K791988.

Who is the listed applicant for REPL. PISTON FOR TROUTMAN CORNEAL PUNCH?

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 REPL. PISTON FOR TROUTMAN CORNEAL PUNCH?

The FDA product code for REPL. PISTON FOR TROUTMAN CORNEAL PUNCH is HNJ.

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.

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Related Devices (Code: HNJ)

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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