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)

PICF 0860/PSCF 0860/PSC 0860/PIAF 0860/PSAF 0860

K-Number: K872731 · 1987-09-15

ApplicantEla Medical, Inc.
Decision Date1987-09-15
Product CodeDTB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

PICF 0860/PSCF 0860/PSC 0860/PIAF 0860/PSAF 0860 is the device name listed in this FDA 510(k) record. The listed applicant is Ela Medical, Inc.. It received FDA 510(k) clearance on 1987-09-15 under 510(k) number K872731. The device is classified under product code DTB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PICF 0860/PSCF 0860/PSC 0860/PIAF 0860/PSAF 0860?

PICF 0860/PSCF 0860/PSC 0860/PIAF 0860/PSAF 0860 is a medical device that received FDA 510(k) clearance on 1987-09-15. The listed applicant is Ela Medical, Inc.. The 510(k) number is K872731.

When did PICF 0860/PSCF 0860/PSC 0860/PIAF 0860/PSAF 0860 receive FDA 510(k) clearance?

PICF 0860/PSCF 0860/PSC 0860/PIAF 0860/PSAF 0860 received FDA 510(k) clearance on 1987-09-15, under 510(k) number K872731.

Who is the listed applicant for PICF 0860/PSCF 0860/PSC 0860/PIAF 0860/PSAF 0860?

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

What is the FDA product code for PICF 0860/PSCF 0860/PSC 0860/PIAF 0860/PSAF 0860?

The FDA product code for PICF 0860/PSCF 0860/PSC 0860/PIAF 0860/PSAF 0860 is DTB.

Other records listing Ela Medical, 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.

K042002SYNESCOPE, EASYSCOPE, SYNECOM, HOLTERREADERK032466SPIDERVIEWK002817SYNETECK993448STELA UT46 AND BT45/46 STRAIGHT TINED PACING LEADS, STELA UJ45 AND BJ44/45 J-SHAPED TINED PACING LEADSK000029STELA UT46 AND BT45/46 STRAIGHT TINED PACING LEADS, STELA UJ45 AND BJ44/45 J-SHAPED TINED PACING LEADSK990727SYNEFLASH & SYNEVIEW

View all 43 devices →

Related Devices (Code: DTB)

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.

K061212BIOTRONIK ENDOCARDIAL PACING LEADSBiotronik, Inc.K041809PERMANENT PACING LEAD, MODEL PY2Oscor, Inc.K040569PERMANENT PACING LEAD, MODEL REFINO, MODEL: REFINO-R, RU, RJUOscor, Inc.K031274MODEL 5071 MYOCARDIAL PACING LEADMedtronic VascularK031210MODEL 4951M MYOCARDIAL UNIPOLAR LEADMetronic, Inc.K023205ELOX P 45-BP; ELOX P 53-BP; ELOX P 60-BPBiotronik, Inc.

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.

↑