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FDA 510(k)

PERIO-TEST

K-Number: K872215 · 1987-07-10

ApplicantDr. Bernard Loewenthal
Decision Date1987-07-10
Product CodeEIL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PERIO-TEST is the device name listed in this FDA 510(k) record. The listed applicant is Dr. Bernard Loewenthal. It received FDA 510(k) clearance on 1987-07-10 under 510(k) number K872215. The device is classified under product code EIL. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERIO-TEST?

PERIO-TEST is a medical device that received FDA 510(k) clearance on 1987-07-10. The listed applicant is Dr. Bernard Loewenthal. The 510(k) number is K872215.

When did PERIO-TEST receive FDA 510(k) clearance?

PERIO-TEST received FDA 510(k) clearance on 1987-07-10, under 510(k) number K872215.

Who is the listed applicant for PERIO-TEST?

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

What is the FDA product code for PERIO-TEST?

The FDA product code for PERIO-TEST is EIL.

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Related Devices (Code: EIL)

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.

K911643ABIODENT PERIOTEMP(R) SYSTEMAbiomed, Inc.K890493FLORIDA PROBE PERIODONTAL PROBEFlorida Probe Corp.K885075ABIOMED PERIOTEMP(TM) PROBEAbiomed, Inc.K884813MODEL 200A ELECTRONIC FORCE-SENSING PROBEVine Valley ResearchK880209PERIODONTAL PROBE - AUTOPROBEDentsply Intl.K872098CREMEEN ALVEOLAR BONE CALIPERBowen & Company, 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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