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FDA 510(k)

CAMPY THIO

K-Number: K792676 · 1980-01-24

ApplicantRemel Co.
Decision Date1980-01-24
Product CodeJSJ
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

CAMPY THIO is the device name listed in this FDA 510(k) record. The listed applicant is Remel Co.. It received FDA 510(k) clearance on 1980-01-24 under 510(k) number K792676. The device is classified under product code JSJ. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAMPY THIO?

CAMPY THIO is a medical device that received FDA 510(k) clearance on 1980-01-24. The listed applicant is Remel Co.. The 510(k) number is K792676.

When did CAMPY THIO receive FDA 510(k) clearance?

CAMPY THIO received FDA 510(k) clearance on 1980-01-24, under 510(k) number K792676.

Who is the listed applicant for CAMPY THIO?

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 CAMPY THIO?

The FDA product code for CAMPY THIO is JSJ.

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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: JSJ)

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.

K882463POTATO DEXTROSE AGAR (PDA) - PRODUCT #P3421Lakewood Biochemical Co., Inc.K881544LITTMAN AGARAcumedia Manufacturers, Inc.K881561TERGITOL 7 BROTHAcumedia Manufacturers, Inc.K881526CHAPMAN STONE MEDIUMAcumedia Manufacturers, Inc.K881571YM BROTHAcumedia Manufacturers, Inc.K881578STREPTOSELAcumedia Manufacturers, 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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