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)

SCISSORS, IRIS

K-Number: K770019 · 1977-01-12

ApplicantJ. Sklar Mfg. Co., Inc.
Decision Date1977-01-12
Product CodeHNF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SCISSORS, IRIS is the device name listed in this FDA 510(k) record. The listed applicant is J. Sklar Mfg. Co., Inc.. It received FDA 510(k) clearance on 1977-01-12 under 510(k) number K770019. The device is classified under product code HNF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCISSORS, IRIS?

SCISSORS, IRIS is a medical device that received FDA 510(k) clearance on 1977-01-12. The listed applicant is J. Sklar Mfg. Co., Inc.. The 510(k) number is K770019.

When did SCISSORS, IRIS receive FDA 510(k) clearance?

SCISSORS, IRIS received FDA 510(k) clearance on 1977-01-12, under 510(k) number K770019.

Who is the listed applicant for SCISSORS, IRIS?

The FDA 510(k) record lists J. Sklar Mfg. Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SCISSORS, IRIS?

The FDA product code for SCISSORS, IRIS is HNF.

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 J. Sklar Mfg. Co., 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.

K843693JACOBS HIGH VACUUM SUCTION UNIT 05-2570K842112TISCHLER CERVICAL BIOPSY PUNCH FORCEPSK842111KOGAN ENDOSPECULUM 9-1/2K822448SCISSORS, VARIOUSK802458KEVORKIAN-YOUNGE BIOPSY CURETTE #90-6611K802457KEVORKIAN-YOUNGE BIOPSY PUNCH, #90-6610

View all 18 devices →

Related Devices (Code: HNF)

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.

K022840STEPHENS DISPOSABLE SCISSORSStephens InstrumentsK897093INTRAOCULAR MICROSCISSORS BY MEANS OF GAMMA RADIA.Microline Pentax, Inc.K873099MANUAL OPHTHALMIC SURGICAL INSTRUMENTSAlcon LaboratoriesK85176813-550,13-560 WESCOTT SCOSSORS (EYE)ArtiberiaK822151SURGICAL INSTRUMENTS REPRESENT. 4 CLASSRobert I. Chien & Assoc., Inc.K821290LITTAUER SCISSORS 5 1/2Conphar, 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.

↑