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)

MINIATURE ASCENDING PAPER CHROMATO-

K-Number: K760908 · 1976-11-19

ApplicantAckerman Nuclear, Inc.
Decision Date1976-11-19
Product CodeDPA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MINIATURE ASCENDING PAPER CHROMATO- is the device name listed in this FDA 510(k) record. The listed applicant is Ackerman Nuclear, Inc.. It received FDA 510(k) clearance on 1976-11-19 under 510(k) number K760908. The device is classified under product code DPA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MINIATURE ASCENDING PAPER CHROMATO-?

MINIATURE ASCENDING PAPER CHROMATO- is a medical device that received FDA 510(k) clearance on 1976-11-19. The listed applicant is Ackerman Nuclear, Inc.. The 510(k) number is K760908.

When did MINIATURE ASCENDING PAPER CHROMATO- receive FDA 510(k) clearance?

MINIATURE ASCENDING PAPER CHROMATO- received FDA 510(k) clearance on 1976-11-19, under 510(k) number K760908.

Who is the listed applicant for MINIATURE ASCENDING PAPER CHROMATO-?

The FDA 510(k) record lists Ackerman Nuclear, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MINIATURE ASCENDING PAPER CHROMATO-?

The FDA product code for MINIATURE ASCENDING PAPER CHROMATO- is DPA.

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

Related Devices (Code: DPA)

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.

K904326DE-TOX TUBES A AND DE-TOX TUBES BDyna-Tek IndustriesK884176CHROMATOGRAPHY KITGelman Sciences, Inc.K791431TECHNICON FAST-LC SYS. FOR THEOPHYLLINETechnicon Instruments Corp.K770765REAGENT SET, RENORPACEG.D. Searle and Co.

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.

↑