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FDA 510(k)

PERIOVIEW MODEL DV-1 FIBERSCOPE AND WINDOW SHEATH.

K-Number: K982480 · 1998-09-15

ApplicantDentalview, Inc.
Decision Date1998-09-15
Product CodeEIA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PERIOVIEW MODEL DV-1 FIBERSCOPE AND WINDOW SHEATH. is the device name listed in this FDA 510(k) record. The listed applicant is Dentalview, Inc.. It received FDA 510(k) clearance on 1998-09-15 under 510(k) number K982480. The device is classified under product code EIA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERIOVIEW MODEL DV-1 FIBERSCOPE AND WINDOW SHEATH.?

PERIOVIEW MODEL DV-1 FIBERSCOPE AND WINDOW SHEATH. is a medical device that received FDA 510(k) clearance on 1998-09-15. The listed applicant is Dentalview, Inc.. The 510(k) number is K982480.

When did PERIOVIEW MODEL DV-1 FIBERSCOPE AND WINDOW SHEATH. receive FDA 510(k) clearance?

PERIOVIEW MODEL DV-1 FIBERSCOPE AND WINDOW SHEATH. received FDA 510(k) clearance on 1998-09-15, under 510(k) number K982480.

Who is the listed applicant for PERIOVIEW MODEL DV-1 FIBERSCOPE AND WINDOW SHEATH.?

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

What is the FDA product code for PERIOVIEW MODEL DV-1 FIBERSCOPE AND WINDOW SHEATH.?

The FDA product code for PERIOVIEW MODEL DV-1 FIBERSCOPE AND WINDOW SHEATH. is EIA.

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 Dentalview, 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.

K973492DENTALVIEW PERIOVIEW SYSTEM

Related Devices (Code: EIA)

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.

K251544Dental Unit (MP2000-550LED-2.0, LP2100-550LED-2.0)Lakong Medical Devices Co., Ltd.K251626Midmark Dental Delivery SystemMidmark CorporationK251491K5 Cart, K5 Mount, K5 SwingOsstem Implant Company., Ltd. Chair BusinessK243130Integral Dental UnitGuangdong Yadeng Medical Apparatus Co., Ltd.,K242611Integral Dental UnitsMipont Medical Equipment Co., Ltd.K250473Dental Delivery System Series 5 and Dental Delivery System Series 5 PlusDci International, LLC

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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