Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

BLOOD ADMINISTRATION TYPE R

K-Number: K771270 · 1977-09-12

ApplicantBerman, Pcp & Consultants, Inc.
Decision Date1977-09-12
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BLOOD ADMINISTRATION TYPE R 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 K771270. 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 BLOOD ADMINISTRATION TYPE R?

BLOOD ADMINISTRATION TYPE R 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 K771270.

When did BLOOD ADMINISTRATION TYPE R receive FDA 510(k) clearance?

BLOOD ADMINISTRATION TYPE R received FDA 510(k) clearance on 1977-09-12, under 510(k) number K771270.

Who is the listed applicant for BLOOD ADMINISTRATION TYPE R?

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 BLOOD ADMINISTRATION TYPE R?

The FDA product code for BLOOD ADMINISTRATION TYPE R 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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.

K771983SCALP VEIN SETK771267INFUSION SET TYPE SK771268INFUSION SET TYPE JK771269BLOOD COLLECTION SET TYPE HK771272DISP. SYRINGES: 2,5 & L0 MI.K771271SCALP VEIN SET

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.

K254123Ecomed Disposable Administration SetsEcomed Solutions, LLCK261530iiSure Infusion SetDeka Research and DevelopmentK252543AMSafe Administration Set (BA-70075, BA-70071-D, BA-70070, BA-70071-P, BA-70072, BA-70072-F, BA-70071-DF, BA-70071-DF-120, FE01, FE04)Amsino International, Inc.K251375PuraCath Firefly Needleless Connector IT (9005)Puracath Medical, Inc.K251257nSet+ Stabilization Set [6426733]; nSet+ Stabilization Set with nSyte Needle Free Connector (NFC) [6426731]; nSyte Needle Free Connector (NFC) [6426727]Np MedicalK250325BD Alaris Pump Infusion SetCarefusion (Bd)

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.

↑