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FDA 510(k)

SULFURIC ACID 10%

K-Number: K872186 · 1987-07-29

ApplicantRemel Co.
Decision Date1987-07-29
Product CodeJTS
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

SULFURIC ACID 10% is the device name listed in this FDA 510(k) record. The listed applicant is Remel Co.. It received FDA 510(k) clearance on 1987-07-29 under 510(k) number K872186. The device is classified under product code JTS. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SULFURIC ACID 10%?

SULFURIC ACID 10% is a medical device that received FDA 510(k) clearance on 1987-07-29. The listed applicant is Remel Co.. The 510(k) number is K872186.

When did SULFURIC ACID 10% receive FDA 510(k) clearance?

SULFURIC ACID 10% received FDA 510(k) clearance on 1987-07-29, under 510(k) number K872186.

Who is the listed applicant for SULFURIC ACID 10%?

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

What is the FDA product code for SULFURIC ACID 10%?

The FDA product code for SULFURIC ACID 10% is JTS.

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Other records listing Remel Co. 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.

K013711BACTI-SWAB DRYK965151A.C.T. IIIK965150A.C.T. IVK965152A.C.T. IIK965149A.C.T. IK960090CALCOFLUOR WHITE STAIN KIT

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Related Devices (Code: JTS)

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.

K960090CALCOFLUOR WHITE STAIN KITRemel Co.K960095BACTIDROP CALCOFLUOR WHITERemel Co.K920970BACTIDROP KOH (10%)Remel Co.K920976BACTIDROP INDIA INKRemel Co.K920975BACTIDROP CALCOFLUOR WHITERemel Co.K893530IRISTAIN FORMULA 2, PARTS 1 AND 2Intl. Remote Imaging Systems

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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