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FDA 510(k)

VKG 1000, VIDEO KERATOMETER

K-Number: K883471 · 1988-11-08

ApplicantTechnitex, Inc.
Decision Date1988-11-08
Product CodeHLP
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

VKG 1000, VIDEO KERATOMETER is the device name listed in this FDA 510(k) record. The listed applicant is Technitex, Inc.. It received FDA 510(k) clearance on 1988-11-08 under 510(k) number K883471. The device is classified under product code HLP. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VKG 1000, VIDEO KERATOMETER?

VKG 1000, VIDEO KERATOMETER is a medical device that received FDA 510(k) clearance on 1988-11-08. The listed applicant is Technitex, Inc.. The 510(k) number is K883471.

When did VKG 1000, VIDEO KERATOMETER receive FDA 510(k) clearance?

VKG 1000, VIDEO KERATOMETER received FDA 510(k) clearance on 1988-11-08, under 510(k) number K883471.

Who is the listed applicant for VKG 1000, VIDEO KERATOMETER?

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

What is the FDA product code for VKG 1000, VIDEO KERATOMETER?

The FDA product code for VKG 1000, VIDEO KERATOMETER is HLP.

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.

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Other records listing Technitex, 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.

K893968VKG 2000 VIDEO KERATOMETERK882902QRK 100, QUALITATIVE RING KERATOSCOPE

Related Devices (Code: HLP)

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.

K874250THREE CHAR. TEST-CHILD & WORTH 4 DOT TEST NEARPT.Richmond Products, Inc.K874251WORTH 4 DOT TEST DISTANCE C/W MUSCLE LIGHTRichmond Products, 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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