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FDA 510(k)

TOOTH PRESERVING SYSTEM

K-Number: K875221 · 1988-04-14

ApplicantBiological Rescue Products, Inc.
Decision Date1988-04-14
Product CodeKJF
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

TOOTH PRESERVING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Biological Rescue Products, Inc.. It received FDA 510(k) clearance on 1988-04-14 under 510(k) number K875221. The device is classified under product code KJF. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TOOTH PRESERVING SYSTEM?

TOOTH PRESERVING SYSTEM is a medical device that received FDA 510(k) clearance on 1988-04-14. The listed applicant is Biological Rescue Products, Inc.. The 510(k) number is K875221.

When did TOOTH PRESERVING SYSTEM receive FDA 510(k) clearance?

TOOTH PRESERVING SYSTEM received FDA 510(k) clearance on 1988-04-14, under 510(k) number K875221.

Who is the listed applicant for TOOTH PRESERVING SYSTEM?

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

What is the FDA product code for TOOTH PRESERVING SYSTEM?

The FDA product code for TOOTH PRESERVING SYSTEM is KJF.

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Related Devices (Code: KJF)

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.

K893787LIFECELL RECOVERY CONTAINERBaxter Healthcare CorpK892645AMICON VITAFIBER FLO-PATH BIORECT/VLS CELL CULT SYAmicon, Inc.K780305CELLDynatech Laboratories, 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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