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FDA 510(k)

KAMPPETER ANOMALOSCOPE

K-Number: K930575 · 1994-02-25

ApplicantBova Intl.
Decision Date1994-02-25
Product CodeHIW
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

KAMPPETER ANOMALOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Bova Intl.. It received FDA 510(k) clearance on 1994-02-25 under 510(k) number K930575. The device is classified under product code HIW. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KAMPPETER ANOMALOSCOPE?

KAMPPETER ANOMALOSCOPE is a medical device that received FDA 510(k) clearance on 1994-02-25. The listed applicant is Bova Intl.. The 510(k) number is K930575.

When did KAMPPETER ANOMALOSCOPE receive FDA 510(k) clearance?

KAMPPETER ANOMALOSCOPE received FDA 510(k) clearance on 1994-02-25, under 510(k) number K930575.

Who is the listed applicant for KAMPPETER ANOMALOSCOPE?

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

What is the FDA product code for KAMPPETER ANOMALOSCOPE?

The FDA product code for KAMPPETER ANOMALOSCOPE is HIW.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Bova Intl. 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.

K930628KLAAS IOL LENSFOLDER

Related Devices (Code: HIW)

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.

K913962ANOMALOSCOPE QUADRANT TEST-6Lkc Technologies, Inc.K860174GUNKEL CHROMAGRAPH COLOR VISION TESTERChromagraphics, Inc.

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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