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FDA 510(k)

LIQUICHEK SERUM VOLATILES CONTROL, MODELS 383 AND 384

K-Number: K984225 · 1998-12-14

ApplicantBio-Rad
Decision Date1998-12-14
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

LIQUICHEK SERUM VOLATILES CONTROL, MODELS 383 AND 384 is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 1998-12-14 under 510(k) number K984225. The device is classified under product code JJY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIQUICHEK SERUM VOLATILES CONTROL, MODELS 383 AND 384?

LIQUICHEK SERUM VOLATILES CONTROL, MODELS 383 AND 384 is a medical device that received FDA 510(k) clearance on 1998-12-14. The listed applicant is Bio-Rad. The 510(k) number is K984225.

When did LIQUICHEK SERUM VOLATILES CONTROL, MODELS 383 AND 384 receive FDA 510(k) clearance?

LIQUICHEK SERUM VOLATILES CONTROL, MODELS 383 AND 384 received FDA 510(k) clearance on 1998-12-14, under 510(k) number K984225.

Who is the listed applicant for LIQUICHEK SERUM VOLATILES CONTROL, MODELS 383 AND 384?

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

What is the FDA product code for LIQUICHEK SERUM VOLATILES CONTROL, MODELS 383 AND 384?

The FDA product code for LIQUICHEK SERUM VOLATILES CONTROL, MODELS 383 AND 384 is JJY.

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Other records listing Bio-Rad as applicant

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Related Devices (Code: JJY)

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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