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FDA 510(k)

VITRECTOMY INTEGRATING TRAY OCUTOME/FRAG

K-Number: K791212 · 1979-08-10

ApplicantPrecision Medical Instruments, Inc.
Decision Date1979-08-10
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

VITRECTOMY INTEGRATING TRAY OCUTOME/FRAG is the device name listed in this FDA 510(k) record. The listed applicant is Precision Medical Instruments, Inc.. It received FDA 510(k) clearance on 1979-08-10 under 510(k) number K791212. The device is classified under product code HQE. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITRECTOMY INTEGRATING TRAY OCUTOME/FRAG?

VITRECTOMY INTEGRATING TRAY OCUTOME/FRAG is a medical device that received FDA 510(k) clearance on 1979-08-10. The listed applicant is Precision Medical Instruments, Inc.. The 510(k) number is K791212.

When did VITRECTOMY INTEGRATING TRAY OCUTOME/FRAG receive FDA 510(k) clearance?

VITRECTOMY INTEGRATING TRAY OCUTOME/FRAG received FDA 510(k) clearance on 1979-08-10, under 510(k) number K791212.

Who is the listed applicant for VITRECTOMY INTEGRATING TRAY OCUTOME/FRAG?

The FDA 510(k) record lists Precision Medical Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VITRECTOMY INTEGRATING TRAY OCUTOME/FRAG?

The FDA product code for VITRECTOMY INTEGRATING TRAY OCUTOME/FRAG is HQE.

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Other records listing Precision Medical Instruments, 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: HQE)

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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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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