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FDA 510(k)

HY PBC FLASK

K-Number: K870133 · 1987-02-05

ApplicantHy Laboratories, Ltd.
Decision Date1987-02-05
Product CodeJSG
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

HY PBC FLASK is the device name listed in this FDA 510(k) record. The listed applicant is Hy Laboratories, Ltd.. It received FDA 510(k) clearance on 1987-02-05 under 510(k) number K870133. The device is classified under product code JSG. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HY PBC FLASK?

HY PBC FLASK is a medical device that received FDA 510(k) clearance on 1987-02-05. The listed applicant is Hy Laboratories, Ltd.. The 510(k) number is K870133.

When did HY PBC FLASK receive FDA 510(k) clearance?

HY PBC FLASK received FDA 510(k) clearance on 1987-02-05, under 510(k) number K870133.

Who is the listed applicant for HY PBC FLASK?

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

What is the FDA product code for HY PBC FLASK?

The FDA product code for HY PBC FLASK is JSG.

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Related Devices (Code: JSG)

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.

K882495THIOGLYCOLLATE BROTH W/VITA. K & HEMIN - #T3007Lakewood Biochemical Co., Inc.K881558TRYPTOSE AGARAcumedia Manufacturers, Inc.K881550OF BASAL MEDIUMAcumedia Manufacturers, Inc.K881557TRYPTONEAcumedia Manufacturers, Inc.K881564TRYPTOSE BLOOD AGAR BASE W/YEAST EXTRACTAcumedia Manufacturers, Inc.K881533BLOOD AGAR BASE NO. 2Acumedia 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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