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FDA 510(k)

DISSECTOR, TROUTMAN CORNEAL

K-Number: K760186 · 1976-08-04

ApplicantV. Mueller O.V. Baxter Healthcare Corp.
Decision Date1976-08-04
Product CodeHNN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

DISSECTOR, TROUTMAN CORNEAL 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 K760186. The device is classified under product code HNN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISSECTOR, TROUTMAN CORNEAL?

DISSECTOR, TROUTMAN CORNEAL 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 K760186.

When did DISSECTOR, TROUTMAN CORNEAL receive FDA 510(k) clearance?

DISSECTOR, TROUTMAN CORNEAL received FDA 510(k) clearance on 1976-08-04, under 510(k) number K760186.

Who is the listed applicant for DISSECTOR, TROUTMAN CORNEAL?

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 DISSECTOR, TROUTMAN CORNEAL?

The FDA product code for DISSECTOR, TROUTMAN CORNEAL is HNN.

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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.

K803292FIELD SUCTION DISSECTORK792383KELMAN DIPSTICKK771197NORTON ENDOTRACHEALK771302PFISTER-SCHWARTZ STONE RETRIEVERK770959BOUGIE, FILIFORM, JACKSONK770280CORD, ELECTROSURGICAL-STERILE & DISPOS.

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Related Devices (Code: HNN)

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.

K110166CLEARCUT S SAFETY KNIFEAlcon Research, Ltd.K922378OPHTHALMIC KNIFEMicroptics Development LaboratoryK882402RETRACTIVE INCISION MICROMETER (RIM) GUAGEOptical CenterK881669MVR/STILETTO BLADE 20GA. - P/N 1900Advanced Surgical Products, Inc.K874979PRISMA DISPOSABLE MVR/STILETTO BLADEAdvanced Surgical Products, Inc.K874057OPHTHALMIC TIP & BLADE SCALPELSMyocure, Inc.

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.

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