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FDA 510(k)

NATIONAL MEDICAL HALTHCARE CUSTOM OPHTHALMIC KITS OR TRAYS

K-Number: K971465 · 1997-06-04

Decision Date1997-06-04
Product CodeHOY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

NATIONAL MEDICAL HALTHCARE CUSTOM OPHTHALMIC KITS OR TRAYS is the device name listed in this FDA 510(k) record. The listed applicant is National Healthcare Mfg. Corp.. It received FDA 510(k) clearance on 1997-06-04 under 510(k) number K971465. The device is classified under product code HOY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NATIONAL MEDICAL HALTHCARE CUSTOM OPHTHALMIC KITS OR TRAYS?

NATIONAL MEDICAL HALTHCARE CUSTOM OPHTHALMIC KITS OR TRAYS is a medical device that received FDA 510(k) clearance on 1997-06-04. The listed applicant is National Healthcare Mfg. Corp.. The 510(k) number is K971465.

When did NATIONAL MEDICAL HALTHCARE CUSTOM OPHTHALMIC KITS OR TRAYS receive FDA 510(k) clearance?

NATIONAL MEDICAL HALTHCARE CUSTOM OPHTHALMIC KITS OR TRAYS received FDA 510(k) clearance on 1997-06-04, under 510(k) number K971465.

Who is the listed applicant for NATIONAL MEDICAL HALTHCARE CUSTOM OPHTHALMIC KITS OR TRAYS?

The FDA 510(k) record lists National Healthcare Mfg. Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NATIONAL MEDICAL HALTHCARE CUSTOM OPHTHALMIC KITS OR TRAYS?

The FDA product code for NATIONAL MEDICAL HALTHCARE CUSTOM OPHTHALMIC KITS OR TRAYS is HOY.

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 National Healthcare Mfg. 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 7 devices →

Related Devices (Code: HOY)

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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