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FDA 510(k)

ORICULT-N CULTURE-PADDLE

K-Number: K872058 · 1987-06-10

ApplicantOrion Corp.
Decision Date1987-06-10
Product CodeJSI
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ORICULT-N CULTURE-PADDLE is the device name listed in this FDA 510(k) record. The listed applicant is Orion Corp.. It received FDA 510(k) clearance on 1987-06-10 under 510(k) number K872058. The device is classified under product code JSI. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORICULT-N CULTURE-PADDLE?

ORICULT-N CULTURE-PADDLE is a medical device that received FDA 510(k) clearance on 1987-06-10. The listed applicant is Orion Corp.. The 510(k) number is K872058.

When did ORICULT-N CULTURE-PADDLE receive FDA 510(k) clearance?

ORICULT-N CULTURE-PADDLE received FDA 510(k) clearance on 1987-06-10, under 510(k) number K872058.

Who is the listed applicant for ORICULT-N CULTURE-PADDLE?

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

What is the FDA product code for ORICULT-N CULTURE-PADDLE?

The FDA product code for ORICULT-N CULTURE-PADDLE is JSI.

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Other records listing Orion Corp. 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.

K912391RUBALEX, MODIFICATIONK901637RESUBMITTED MODIFIED RUBALEXK884650RESUBMITTED SCANORAK890199DENTOCULT SM-STRIP MUTANSK881506MAMEX DC MAG MG12K881505MAMEX DC MG11

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Related Devices (Code: JSI)

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.

K070691BBL CHROMAGAR 0157Becton, Dickinson & COK974428DIPSTREAKNovamed , Ltd.K891593LISTERIA SELECTIVE ENRICHMENT MEDIUMOxoid U.S.A., Inc.K890199DENTOCULT SM-STRIP MUTANSOrion Corp.K882182SALMONELLA-SHIGELLA (SS) AGAR - PRODUCT #P3326Lakewood Biochemical Co., Inc.K881575SELECTIVE STREPTOCOCCUS AGARAcumedia 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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