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FDA 510(k)

MCDONALD FOLDING FORCEPS

K-Number: K885230 · 1989-05-17

Decision Date1989-05-17
Product CodeHNR
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MCDONALD FOLDING FORCEPS is the device name listed in this FDA 510(k) record. The listed applicant is Alcon Laboratories. It received FDA 510(k) clearance on 1989-05-17 under 510(k) number K885230. 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 MCDONALD FOLDING FORCEPS?

MCDONALD FOLDING FORCEPS is a medical device that received FDA 510(k) clearance on 1989-05-17. The listed applicant is Alcon Laboratories. The 510(k) number is K885230.

When did MCDONALD FOLDING FORCEPS receive FDA 510(k) clearance?

MCDONALD FOLDING FORCEPS received FDA 510(k) clearance on 1989-05-17, under 510(k) number K885230.

Who is the listed applicant for MCDONALD FOLDING FORCEPS?

The FDA 510(k) record lists Alcon Laboratories as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MCDONALD FOLDING FORCEPS?

The FDA product code for MCDONALD FOLDING 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 Alcon Laboratories 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 47 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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