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FDA 510(k)

SCISSORS, MICRO IRIS CURVED

K-Number: K760188 · 1976-08-04

Decision Date1976-08-04
Product CodeHNF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SCISSORS, MICRO IRIS CURVED is the device name listed in this FDA 510(k) record. The listed applicant is V. Mueller O.V. Baxter Healthcare Corp.. It received FDA 510(k) clearance on 1976-08-04 under 510(k) number K760188. The device is classified under product code HNF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCISSORS, MICRO IRIS CURVED?

SCISSORS, MICRO IRIS CURVED is a medical device that received FDA 510(k) clearance on 1976-08-04. The listed applicant is V. Mueller O.V. Baxter Healthcare Corp.. The 510(k) number is K760188.

When did SCISSORS, MICRO IRIS CURVED receive FDA 510(k) clearance?

SCISSORS, MICRO IRIS CURVED received FDA 510(k) clearance on 1976-08-04, under 510(k) number K760188.

Who is the listed applicant for SCISSORS, MICRO IRIS CURVED?

The FDA 510(k) record lists V. Mueller O.V. Baxter Healthcare Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SCISSORS, MICRO IRIS CURVED?

The FDA product code for SCISSORS, MICRO IRIS CURVED is HNF.

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 V. Mueller O.V. Baxter Healthcare Corp. 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 41 devices →

Related Devices (Code: HNF)

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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