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FDA 510(k)

SYNALON ROLLER BOTTLE

K-Number: K791049 · 1979-06-28

ApplicantDynatech Laboratories, Inc.
Decision Date1979-06-28
Product CodeKJC
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

SYNALON ROLLER BOTTLE is the device name listed in this FDA 510(k) record. The listed applicant is Dynatech Laboratories, Inc.. It received FDA 510(k) clearance on 1979-06-28 under 510(k) number K791049. 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 SYNALON ROLLER BOTTLE?

SYNALON ROLLER BOTTLE is a medical device that received FDA 510(k) clearance on 1979-06-28. The listed applicant is Dynatech Laboratories, Inc.. The 510(k) number is K791049.

When did SYNALON ROLLER BOTTLE receive FDA 510(k) clearance?

SYNALON ROLLER BOTTLE received FDA 510(k) clearance on 1979-06-28, under 510(k) number K791049.

Who is the listed applicant for SYNALON ROLLER BOTTLE?

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

What is the FDA product code for SYNALON ROLLER BOTTLE?

The FDA product code for SYNALON 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.K873137IN VITRO 2.5X ROLLER BOTTLEIn Vitro Scientific Products

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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