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FDA 510(k)

INFUSION SET TYPE J

K-Number: K771268 · 1977-09-12

Decision Date1977-09-12
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

INFUSION SET TYPE J is the device name listed in this FDA 510(k) record. The listed applicant is Berman, Pcp & Consultants, Inc.. It received FDA 510(k) clearance on 1977-09-12 under 510(k) number K771268. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INFUSION SET TYPE J?

INFUSION SET TYPE J is a medical device that received FDA 510(k) clearance on 1977-09-12. The listed applicant is Berman, Pcp & Consultants, Inc.. The 510(k) number is K771268.

When did INFUSION SET TYPE J receive FDA 510(k) clearance?

INFUSION SET TYPE J received FDA 510(k) clearance on 1977-09-12, under 510(k) number K771268.

Who is the listed applicant for INFUSION SET TYPE J?

The FDA 510(k) record lists Berman, Pcp & Consultants, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INFUSION SET TYPE J?

The FDA product code for INFUSION SET TYPE J is FPA.

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 Berman, Pcp & Consultants, Inc. 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 7 devices →

Related Devices (Code: FPA)

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

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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