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FDA 510(k)

COULTER VISCOMETER II

K-Number: K883503 · 1988-09-19

ApplicantCoulter Electronics, Inc.
Decision Date1988-09-19
Product CodeJJL
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

COULTER VISCOMETER II is the device name listed in this FDA 510(k) record. The listed applicant is Coulter Electronics, Inc.. It received FDA 510(k) clearance on 1988-09-19 under 510(k) number K883503. The device is classified under product code JJL. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COULTER VISCOMETER II?

COULTER VISCOMETER II is a medical device that received FDA 510(k) clearance on 1988-09-19. The listed applicant is Coulter Electronics, Inc.. The 510(k) number is K883503.

When did COULTER VISCOMETER II receive FDA 510(k) clearance?

COULTER VISCOMETER II received FDA 510(k) clearance on 1988-09-19, under 510(k) number K883503.

Who is the listed applicant for COULTER VISCOMETER II?

The FDA 510(k) record lists Coulter Electronics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COULTER VISCOMETER II?

The FDA product code for COULTER VISCOMETER II is JJL.

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Other records listing Coulter Electronics, Inc. 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.

K923951CD8 CYTOSPHERES KITK930119COULTER RETIC-C CELL CONTROLK921279CD4 CYTOSPHERES KITK923530COULTER MULTI-Q-PREPK922181COULTER MH009K922704COULTER MAXM W/ AUTOLOADER

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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