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FDA 510(k)

TISSUE CULTURE FLASK PL 732 PLASTIC ACCESSORY PROD

K-Number: K862152 · 1986-06-16

Decision Date1986-06-16
Product CodeKJA
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

TISSUE CULTURE FLASK PL 732 PLASTIC ACCESSORY PROD is the device name listed in this FDA 510(k) record. The listed applicant is Travenol Laboratories, S.A.. It received FDA 510(k) clearance on 1986-06-16 under 510(k) number K862152. The device is classified under product code KJA. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TISSUE CULTURE FLASK PL 732 PLASTIC ACCESSORY PROD?

TISSUE CULTURE FLASK PL 732 PLASTIC ACCESSORY PROD is a medical device that received FDA 510(k) clearance on 1986-06-16. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K862152.

When did TISSUE CULTURE FLASK PL 732 PLASTIC ACCESSORY PROD receive FDA 510(k) clearance?

TISSUE CULTURE FLASK PL 732 PLASTIC ACCESSORY PROD received FDA 510(k) clearance on 1986-06-16, under 510(k) number K862152.

Who is the listed applicant for TISSUE CULTURE FLASK PL 732 PLASTIC ACCESSORY PROD?

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

What is the FDA product code for TISSUE CULTURE FLASK PL 732 PLASTIC ACCESSORY PROD?

The FDA product code for TISSUE CULTURE FLASK PL 732 PLASTIC ACCESSORY PROD is KJA.

Related Clinical Trials

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.

Other records listing Travenol Laboratories, S.A. 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.

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Related Devices (Code: KJA)

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.

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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