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FDA 510(k)

SUCROSE

K-Number: K820214 · 1982-02-05

ApplicantDms Laboratories
Decision Date1982-02-05
Product CodeJSE
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SUCROSE is the device name listed in this FDA 510(k) record. The listed applicant is Dms Laboratories. It received FDA 510(k) clearance on 1982-02-05 under 510(k) number K820214. The device is classified under product code JSE. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUCROSE?

SUCROSE is a medical device that received FDA 510(k) clearance on 1982-02-05. The listed applicant is Dms Laboratories. The 510(k) number is K820214.

When did SUCROSE receive FDA 510(k) clearance?

SUCROSE received FDA 510(k) clearance on 1982-02-05, under 510(k) number K820214.

Who is the listed applicant for SUCROSE?

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

What is the FDA product code for SUCROSE?

The FDA product code for SUCROSE is JSE.

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Other records listing Dms Laboratories 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.

K831187TRPK831186RAPID NFTK830437CHSK823102AGAR PK821038FAST VIOLET BK813613RAPID CH

View all 23 devices →

Related Devices (Code: JSE)

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.

K962265MLX MICROTITER PLATE LUMINOMETERDynatech Laboratories, Inc.K883995X-ACT UREA/TDAPro-Lab, Inc.K883996X-ACT LDC/INDPro-Lab, Inc.K880133MIL MEDIUMHardy MediaK880116MRVP BROTHHardy MediaK874537KLIGLER IRON AGAR AND TRIPLE SUGAR IRON AGARLakewood Biochemical Co., 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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