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FDA 510(k)

19091-XXXXX SER. OF GLASS CAPILLARY COL.

K-Number: K791893 · 1979-10-30

Decision Date1979-10-30
Product CodeDII
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

19091-XXXXX SER. OF GLASS CAPILLARY COL. is the device name listed in this FDA 510(k) record. The listed applicant is Hewlett-Packard Co.. It received FDA 510(k) clearance on 1979-10-30 under 510(k) number K791893. The device is classified under product code DII. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 19091-XXXXX SER. OF GLASS CAPILLARY COL.?

19091-XXXXX SER. OF GLASS CAPILLARY COL. is a medical device that received FDA 510(k) clearance on 1979-10-30. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K791893.

When did 19091-XXXXX SER. OF GLASS CAPILLARY COL. receive FDA 510(k) clearance?

19091-XXXXX SER. OF GLASS CAPILLARY COL. received FDA 510(k) clearance on 1979-10-30, under 510(k) number K791893.

Who is the listed applicant for 19091-XXXXX SER. OF GLASS CAPILLARY COL.?

The FDA 510(k) record lists Hewlett-Packard Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 19091-XXXXX SER. OF GLASS CAPILLARY COL.?

The FDA product code for 19091-XXXXX SER. OF GLASS CAPILLARY COL. is DII.

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 Hewlett-Packard Co. 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.

View all 230 devices →

Related Devices (Code: DII)

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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