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FDA 510(k)

BERTHOLD LB 2103,2104-XT/PC/AT,951G GAMMA COUNTERS

K-Number: K870115 · 1987-03-31

ApplicantBerthold Analytical Instruments, Inc.
Decision Date1987-03-31
Product CodeJJJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BERTHOLD LB 2103,2104-XT/PC/AT,951G GAMMA COUNTERS is the device name listed in this FDA 510(k) record. The listed applicant is Berthold Analytical Instruments, Inc.. It received FDA 510(k) clearance on 1987-03-31 under 510(k) number K870115. The device is classified under product code JJJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BERTHOLD LB 2103,2104-XT/PC/AT,951G GAMMA COUNTERS?

BERTHOLD LB 2103,2104-XT/PC/AT,951G GAMMA COUNTERS is a medical device that received FDA 510(k) clearance on 1987-03-31. The listed applicant is Berthold Analytical Instruments, Inc.. The 510(k) number is K870115.

When did BERTHOLD LB 2103,2104-XT/PC/AT,951G GAMMA COUNTERS receive FDA 510(k) clearance?

BERTHOLD LB 2103,2104-XT/PC/AT,951G GAMMA COUNTERS received FDA 510(k) clearance on 1987-03-31, under 510(k) number K870115.

Who is the listed applicant for BERTHOLD LB 2103,2104-XT/PC/AT,951G GAMMA COUNTERS?

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

What is the FDA product code for BERTHOLD LB 2103,2104-XT/PC/AT,951G GAMMA COUNTERS?

The FDA product code for BERTHOLD LB 2103,2104-XT/PC/AT,951G GAMMA COUNTERS is JJJ.

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 Berthold Analytical Instruments, 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.

K872324LB 9502 - CLINILUMAT, LB 952 - AUTO-CLINILUMAT

Related Devices (Code: JJJ)

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.

K962762SEQUENTIAL SAMPLE MULTI-PHOTON DETECTORBiotraces, Inc.K946387CAPRA (CAPRAC-R) WIPETEST AND WELL COUNTERCapintec, Inc.K920559ABBOTT VERTEX ANALYZERAbbott LaboratoriesK900087GENESYS 6000 GAMMA COUNTERLaboratory Technologies, Inc.K896202MATRIX(TM)-96Canberra Industries, Inc.K894902SOURCEREROakfield Instruments, Ltd.

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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