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FDA 510(k)

IN VITRO 2.5X ROLLER BOTTLE

K-Number: K873137 · 1987-08-24

ApplicantIn Vitro Scientific Products
Decision Date1987-08-24
Product CodeKJC
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

IN VITRO 2.5X ROLLER BOTTLE is the device name listed in this FDA 510(k) record. The listed applicant is In Vitro Scientific Products. It received FDA 510(k) clearance on 1987-08-24 under 510(k) number K873137. The device is classified under product code KJC. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IN VITRO 2.5X ROLLER BOTTLE?

IN VITRO 2.5X ROLLER BOTTLE is a medical device that received FDA 510(k) clearance on 1987-08-24. The listed applicant is In Vitro Scientific Products. The 510(k) number is K873137.

When did IN VITRO 2.5X ROLLER BOTTLE receive FDA 510(k) clearance?

IN VITRO 2.5X ROLLER BOTTLE received FDA 510(k) clearance on 1987-08-24, under 510(k) number K873137.

Who is the listed applicant for IN VITRO 2.5X ROLLER BOTTLE?

The FDA 510(k) record lists In Vitro Scientific Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IN VITRO 2.5X ROLLER BOTTLE?

The FDA product code for IN VITRO 2.5X ROLLER BOTTLE is KJC.

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Related Devices (Code: KJC)

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.

K880509MULTISURFACE ROLLER BOTTLE (M.S.R.B.)Motil Plastics , Ltd.K791049SYNALON ROLLER BOTTLEDynatech Laboratories, 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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