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FDA 510(k)

CREMEEN ALVEOLAR BONE CALIPER

K-Number: K872098 · 1987-07-31

ApplicantBowen & Company, Inc.
Decision Date1987-07-31
Product CodeEIL
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CREMEEN ALVEOLAR BONE CALIPER is the device name listed in this FDA 510(k) record. The listed applicant is Bowen & Company, Inc.. It received FDA 510(k) clearance on 1987-07-31 under 510(k) number K872098. 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 CREMEEN ALVEOLAR BONE CALIPER?

CREMEEN ALVEOLAR BONE CALIPER is a medical device that received FDA 510(k) clearance on 1987-07-31. The listed applicant is Bowen & Company, Inc.. The 510(k) number is K872098.

When did CREMEEN ALVEOLAR BONE CALIPER receive FDA 510(k) clearance?

CREMEEN ALVEOLAR BONE CALIPER received FDA 510(k) clearance on 1987-07-31, under 510(k) number K872098.

Who is the listed applicant for CREMEEN ALVEOLAR BONE CALIPER?

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

What is the FDA product code for CREMEEN ALVEOLAR BONE CALIPER?

The FDA product code for CREMEEN ALVEOLAR BONE CALIPER is EIL.

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Other records listing Bowen & Company, 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.

K896898BOWEN ELECTRODE SKIN PREPATORY CLEANSERK896538DISPOSABLE 45 DEGREE SHAVERK873766STERNAL POWER AWLK871325BOWEN REUSEABLE/DISPOSABLE ELECTRODEK870881LOOSE BODY GRASPERSK87088245 DEGREE SHAVER

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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.K872215PERIO-TESTDr. Bernard Loewenthal

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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