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FDA 510(k)

DC-BILITROL CATALOGUE # SE-021, SE-022, SE-023

K-Number: K882259 · 1988-07-21

ApplicantDiagnostic Chemicals, Ltd. (Usa)
Decision Date1988-07-21
Product CodeJIT
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

DC-BILITROL CATALOGUE # SE-021, SE-022, SE-023 is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Chemicals, Ltd. (Usa). It received FDA 510(k) clearance on 1988-07-21 under 510(k) number K882259. The device is classified under product code JIT. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DC-BILITROL CATALOGUE # SE-021, SE-022, SE-023?

DC-BILITROL CATALOGUE # SE-021, SE-022, SE-023 is a medical device that received FDA 510(k) clearance on 1988-07-21. The listed applicant is Diagnostic Chemicals, Ltd. (Usa). The 510(k) number is K882259.

When did DC-BILITROL CATALOGUE # SE-021, SE-022, SE-023 receive FDA 510(k) clearance?

DC-BILITROL CATALOGUE # SE-021, SE-022, SE-023 received FDA 510(k) clearance on 1988-07-21, under 510(k) number K882259.

Who is the listed applicant for DC-BILITROL CATALOGUE # SE-021, SE-022, SE-023?

The FDA 510(k) record lists Diagnostic Chemicals, Ltd. (Usa) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DC-BILITROL CATALOGUE # SE-021, SE-022, SE-023?

The FDA product code for DC-BILITROL CATALOGUE # SE-021, SE-022, SE-023 is JIT.

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Other records listing Diagnostic Chemicals, Ltd. (Usa) 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.

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Related Devices (Code: JIT)

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.

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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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